The Office of Research and Project Administration (ORPA) plays a critical role in the development and submission of research funding proposals, the management of institutional and external research funds, and the fiscal management of clinical trials at MSK. We are currently seeking an ORPA Coordinator to oversee processes and projects with a high level of complexity, visibility, and impact that involve all 5 business units of ORPA as well as the larger SKI research community. You Will: - Serve as System Administrator for the central grants management system, fielding questions and troubleshooting system issues for RTM and the SKI research community- Oversee the SKI fund establishment process, including QA review of new funds, creation of institutional funds, and verification of supporting information- Manage the Internal Competition proposal submission system and workflow, including training the research community on the Internal Competition process, and serving as the central point of contact for questions and issues- Monitor and analyze grant and HR data used by internal and external clients in support of operational decisions and the SKI research community- Produce and review reports to monitor data integrity; report anomalies (e.g. incorrect, incomplete or missing information) to appropriate staff for follow-up and correction- Play a lead role in projects related to new system implementation and/or upgrades to existing systems, including design, testing, rollout and training - Maintain accurate and up-to-date information in systems and on ORPA website and TeamShare You Are:- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances- Adept at creating partnerships and working collaboratively to meet shared objectives and goals- Capable of building strong customer relationships and delivering customer-centric solutions- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward- Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm- Able to deftly navigate communication amongst varying work styles for effective outcomes You Have: - Bachelor's degree- 2-4 years of experience in an office setting with a strong knowledge of computer systems and software- Strong understanding of grants management, or experience in an academic research setting preferred #LI-Post
The Office of Research and Project Administration (ORPA) plays a crucial role for all activities related to the management of institutional and external research funds, and the development and submission of funding proposals. ORPA is currently seeking a dynamic leader to manage a growing team of grants managers (GMs) in the Grants & Contracts unit dedicated to maximizing external research funding support for MSK investigators. Reporting to the Director, Grants & Contracts, as the Manager, Grants & Contracts, you will:- Hold a leadership role on the ORPA management team, leading and managing high-level projects, generating team resources and developing staff.- Provide operational guidance to the GMs to ensure and facilitate efficient and effective daily operations of the Grants & Contracts Unit.- Lead recruitment efforts for new team members and make recommendations for hire. Orient, train and evaluate staff performance.- Obtain, analyze and communicate data necessary for fulfilling unit, department or institutional needs. Monitor unit-specific key performance indicators and metrics; propose and implement new business plans and procedures to improve overall efficiency of the grants management team. Make recommendations to the Director regarding departmental operations based on analysis of information.- Lead and assist with projects and administrative initiatives as assigned by the Director and Vice President. Partner with departmental and divisional colleagues, MSK faculty, administrative and clinical management staff to plan and implement new department-wide, and divisional or institutional programmatic initiatives related to pre-award and non-financial post award management of sponsored research at MSK.- Plan, develop and implement or participate in assigned projects with department and/or institutional impact; develop and sustain project flows and timelines, seeking guidance from and provide progress reports to the Director and Vice President, as required.You Are:- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward.- Focused on continuous improvement, knowing the most effective and efficient processes to optimize work flow. - Eager to foster talent and support people in meeting their career goals and the organization's goals.- Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- Knowledgeable about business and the marketplace and able to apply this knowledge to advance the organization's goals.- Able to work effectively in an environment notable for complex, sometimes contradictory information. - Adept at creating partnerships and working collaboratively with others to meet shared objectives and goalsYou have:- A Bachelor’s Degree (Master’s preferred).- Five years of research administration experience.- Two years of supervisory experience. - The ability to develop, facilitate, and orchestrate effective communication with all members of the Center; responsible for writing, preparing, and educating staff on grants and contracting procedures and processes.- Solid experience interacting with all levels of staff including clinical/research staff (investigators, etc), administration, research and clerical support staff, and institutional leaders.- The ability to apply broad technical and professional knowledge, and significant job-related experience to function as an internal consultant and assume managerial responsibility in a specialized functional unit of the organization.- Experience with the development and submission of governmental research grant applications, preferably to federal agencies like the National Institutes of Health.- Certified Research Administrator (CRA) or Certified Pre-Award Research Administrator (CPRA) preferred. #LI-POST
We are currently seeking a Senior Grants Manager to join our Grants and Contracts team. Our Grants and Contracts department, a unit of the Office of Research and Project Administration (ORPA), manages the pre-award administration of research grants and contracts funded by federal, state, and private agencies. As a Senior Grants Manager you will:- Be a self-directed professional responsible for providing customer-focused support to investigators by managing day-to-day activities associated with pre-award and non-financial post-award management of sponsored research proposals and awards, including, but not limited to government, non-government and other sponsors- Authorize and submit proposals to external sponsors on behalf of MSK's Authorized Organizational Representative- Act as a consultant for MSK faculty on matters related to the management of their grants portfolio- Serve as a the primary institutional liaison between MSK and external sponsors and coordinates with other central offices and collaborating sites on behalf of investigators to support coordinated management of their grants portfolio- Ensure institutional compliance with federal, state, agency and other applicable governing regulations, policies and procedures concerning sponsored researchYou are:- Self-motivated, willing to take action, individual, with demonstrated ability to establish relationships, prioritize and multi-task on parallel projects- Customer-focused and interested in collaboration- Able to adapt in ambiguous situations and produce results - Adept at planning and prioritizing to work within tight timeframes and meet strict deadlines- A strong communicator with high level of interpersonal and oral communication skills and able to easily interact with a diverse group of individuals- Someone confident and able to effectively engage stakeholders in challenging or deadline-oriented situations- Demonstrates a high level of initiative and ability to work with minimum supervision; requires minimal guidance when addressing complex issues.- Able to manage workload and lead high priority projectsYou have: - A Bachelor’s Degree with a minimum of 4-7 years’ experience in a related field, ideally in a research administration environment performing duties similar to the above. 7-10 years of directly related experience may be substituted for the degree- Experience showing progressive increases in responsibility, the ability to develop and complete projects with minimal supervision, and will have demonstrated skills in working effectively with faculty, staff and external agencies.- Experience reading and interpreting funding opportunity announcements or similar, demonstrated knowledge of pre-award grant submission process and federal application requirements and policy regulations are highly preferred.- Knowledge of NIH application requirements and policy regulations and a familiarity with web based submission software (e.g. Cayuse) also highly preferred.LI-POST
The Information Services team is looking for an Virtualization/Cloud Engineer to join a collaborative server infrastructure team for Memorial Sloan Kettering’s enterprise datacenter. The position provides the opportunity to manage enterprise-class VMware and Microsoft platforms using the latest HP and Cisco server hardware, allowing us to provide highly-available solutions that meet our organizational requirements. - Demonstrate enterprise-level expertise in VMware infrastructure technologies and methodologies to include but not limited to, vSphere, vCenter, vSAN, vROPS, performance tuning, capacity planning, and issue diagnosis.- Demonstrate enterprise-level expertise in server hardware knowledge and hands-on experience, especially with Cisco UCS B and C Series Servers, Fabric Interconnects, UCS Central and UCS Manager as well as firmware/driver relationships.- Demonstrate expertise in operating systems for virtual platforms.- Provide level 3 technical support for complex infrastructure issues.- Possess a broad understanding of networking and SAN technologies and concepts.- Proactively identify system deficiencies and performance bottlenecks by generating system metrics and reports; suggest and execute corrective changes- Identify areas where existing policies, procedures, or configurations require change or where new ones need to be developed- Review critical customer platform advisories, assess their potential impact to our existing infrastructure, and suggest steps to remediate- Assist team architects in the evaluation of new products, solutions, and services- Ability to work independently and/or in a team setting, and with a high level of attention to detail.- Effectively communicate technical topics with other IT foundational groups, product vendors, management, and stakeholders.- Ability to manage several project simultaneously and prioritize tasks accordingly- Accurately report progress of assigned tasks; meet commitments and project due dates; effective planning and foresight to mitigate potential delays- Required to participate in rotating 24x7 on-call schedule as level 3 escalation point.- Work occasional non-business hours in support of infrastructure and application maintenance (outages, upgrades, etc.The Infrastructure Engineer has:- Bachelor’s degree in related field or 10+ years of related IT experience- Excellent verbal / written interpersonal, presentation, and customer service skills- Proficient in core client applications necessary to communicate and document (MS Office, Visio)- Cloud experience is required- HP, VMware, Microsoft MCSE certifications- Good scripting and programming skills (PowerShell / PowerCLI)- Knowledge of team-adjacent applications such as AD, DNS, SQL, SharePoint, IIS, XenApp, Avamar, etc.#LI-POST
The Financial Analytics and Reporting team at MSK is responsible for developing and providing all financial and management reports to the senior management and supporting finance administration. As our Financial Analytics Manager, you will be our Data, Application Insight and Integration Architect leading our efforts to standardize and improve our platform to support MSK’s financial and operational initiatives. You will manage the full development life cycle of complex projects requiring data integration to other systems including analysis, design, programming, implementation and support. You will influence, shape and innovate solutions to exponentially reduce the time-to-insight for finance management. You will!- Be the technical leader for the planning, analysis, design, data modelling, programming, testing, and deployment of financial analytics, reporting and dashboard solutions for financial officers and other administrative support personnel.- Provide subject matter expertise regarding financial analytics, reporting and dashboard design and/or selection and implementation coordination and addressing multiple system and data integration issues.- Collaborate with business and technical owners to design, build and deploy data pipelines to/from various data sources, including the enterprise data warehouse.- Lead a team of Financial Analytics Specialists to support and maintain analytics platforms.- Contribute to Big Data and analytical discussions, lead business and IT stakeholders through designing a robust, secure and optimized architectures and ability to be hands-on delivering the target solution.- Participate in the definition of technical standards and guidelines that pertain to data and information-use, security, access and governance.- Ensure existing data/information assets are identified, stewarded, governed and leveraged across the enterprise. - Influence related processes among user groups to ensure efficiency.- Work with multi-functional teams to design and implement business requirements.- Develop detailed system and application specifications, including data conversion, interfaces, and custom reporting to ensure business requirements are met.- Manage and track the status of requirements throughout the project lifecycle; enforce and redefine as necessary.- Review, prioritize and track progress of issues that affect the project deliverables.- Guide project team members and monitor progress for assigned projects to assure deadline, standards, and cost target are met.- Ensure compatibility and consistency with enterprise standards including integration of related projects and adjustments to project scope.You need!- 7+ years of Information Systems experience, at least five years of data architecture experience, including business analytics, dashboard and reporting platforms including IBM Cognos and Tableau.- Minimum four (4) years report development or SQL writing or programming experience.- Experience with public cloud data platforms such as Azure (SQL DW, Data Lake, Data Factory), AWS (Redshift, or S3 Data Lake).- BA/BS in Computer Science, Information Technology, technical discipline or equivalent experience is required.- Ability to lead multi-functional teams and communicate well.- Ability to perform business analysis- Ability to stay focused under pressure, prioritizing and running multiple projects simultaneously in a fast-paced environment.- Healthcare industry experience is a strong plus but not required#LI-POST
In this role, you'll work with the Quality and Safety Systems Team and other stakeholders to continuously improve the data management backlog and the development of technologies in support of key patient safety programs. You'll work with a cross-functional team to refine and maintain analytical and digital assets which are intended to accelerate improvements primarily focused on our quality and safety initiatives. This role will provide a dynamic interface to management and staff in support of digital patient safety strategies. This is a high visibility role that provides you the opportunity to impact the lives of MSK patients. Your efforts will be key in identifying, assessing and defining new technology collaboration.What you'll do: - Partner with management on the overall vision and program backlog to create the delivery backlog and prioritize epics and stories- Influencing sequencing of stories into sprints during planning sessions to ensure the quickest delivery of the best member experience and of the maximized business value- Facilitate daily stand-ups, scrum ceremonies, and scrum boards- Facilitate discussion between potential partners and key stakeholders while also helping define timelines- Support the progress of each project by working with internal stakeholders to monitor timelines & deliverablesWho you are: - 2-4 years consulting, product or program management experience- Resilient, action-oriented, and able to manage complexity- Knowledge of Agile methodologies/SAFe or Lean Six Sigma a strong plus- Experience with software development, coding languages (such as .net, python, Java), testing, quality assurance- Knowledge of data tools such as R, SQL, SAS and/or data visualization (e.g. Tableau) tools- Analytics knowledge a plus; we’re excited to enhance your skills!- Comfortable working in virtual environments using a variety of collaboration tools: Teamwork, Teams, Slack, Azure, etc.- Bachelor’s Degree (Master’s preferred) or work experience in lieuLocation: NYC - Midtown East near Grand Central Benefits Competitive compensation packages | Sick Time | Generous Vacation + 12 holidays to recharge & refuel | Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care | 403b retirement savings plan match | Tuition Reimbursement | Parental Leave & Adoption Assistance | Commuter Spending Account | Fitness Discounts & Wellness Program | Resource Networks | Life Insurance & Disability | Remote Flexibility We belive in communication, transparency, and thinking beyond your 8-hour day @ MSK. It’s important to us that you have a sense of impact, community, and work/life balance to be and feel your best. Our Hiring Process You read the ad, agree it sounds like a great fit & apply -> Talent Acquisition contacts you to schedule a phone interview (if your profile aligns) ->after speaking with the Talent Acquisition Specialist, you will connect with the Hiring Manager by phone or video call -> if your experience is a fit, you will move forward to an on-site visit with the team -> post interview feedback -> ideally an offer! -> reference check & onboarding -> orientation & official welcome to MSK We look forward to meeting you soon!#LI-POST
A critical member of the Human Research Protection (HRP) Office within the Protocol Activation and HRPP Unit in Clinical Research Administration (CRA), this position provides operational, technical, administrative leadership and expertise in Institutional Review Board/Privacy Board review committee management and oversight to support the achievement of Center goals for Time to Activation and most importantly to ensure the rights and welfare of MSK's research participants are protected. This position is a leader charged with the operational oversight and management of the IRB/PB, and must ensure full compliance with Institutional, State and Federal regulations (i.e. FDA, Office of Human Research Protections, Office of Civil Rights) and guidances regarding human subjects' protection, AAHRPP(Association for the Accreditation of Human Research Protection Programs) requirements, and others as needed. You Will: - Lead the IRB/PB administration team on the day-to-day operational activities as they relate to the IRB/PB Committee meetings. - Manage the IRB agenda including organizing and finalizing that requires utilizing critical thinking and working knowledge of regulations ensure content is aligned with federal regulations and IRB/PB SOPs.- Co-manage the IRB administration staff (e.g. IRB Analysts, Coordinators) with the other IRB/PB Administrator.- Facilitate IRB/PB Meeting with Chair and/or Co-Chairs, documenting all discussions and actions in accordance with regulations and IRB/PB SOPs.- Write and ensure completion of communications (actions, determination letters-outcomes) in the specified turnaround time. - Provide regulatory guidance to MSK Investigators and clinical research (CR) staff. - Review non-compliance reporting and oversees the real-time management of IRB submissions that must be processed immediately due to patient care needs (e.g., Emergency/Compassionate Use, Prospective Deviations).- Define metrics for determining progress/success. Provides specialized queries, reports and graphical presentations to leadership. - Train IRB/PB members, clinical research teams and HRPP staff, as required. You Have: - A Bachelor’s degree with at least 4 years of clinical research/ human subjects protection experience required, Master’s preferred.- Experience in staff supervision and management preferred.- Previous HSP/IRB experience in oncology setting highly preferred.- Certified IRB Professional (CIP) expected after a minimum of one year in the job based on certification requirements and years of prior IRB experience.- Federal Regulations: Must have an advanced comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA).- Administrative Skills: Excellent administrative skills. Detail-oriented with the ability to multi-task and prioritize workload. Good organizational skills needed.- Communication Skills: Excellent communication skills both oral (for presentations and with contacts) and written (e.g., letters, memorandums). Ability to interact with a diverse group of individuals (e.g., physician leaders, investigators, Committee Chairmen, research management and research support staff).- Analytical Skills: Ability to analyze and draw conclusions from information received and to be able to convey the information to others. Ability to comprehend and apply regulations and SOPs to information presented for consideration by the IRB. Ability to exercise independent judgment and discretion and trouble-shoot without much direction. Excellent problem-solving ability. - Computer Skills: Excellent computer skills. Proficient in Microsoft Office programs (Word, Excel, Access, and Outlook) and relational databases. Familiarity with Adobe software and Crystal Reports.
Are you passionate about the challenge to cure Cancer? Did you know that you can apply your technical skills to support our mission here? The Clinical Bioinformatics group within the department of Pathology specializes in analyzing next-generation sequencing data to characterize the spectrum of genetic mutations in patient tumors. Analysis of this genomic data is guiding treatment decisions and the enrollment of patients onto clinical trials of novel targeted therapies. The clinical data at our group has rapidly grown from 40TB to a private cloud of 2PB, and is managed by over a dozen production servers that facilitate automatic processing of terabytes of data per day, high-end intensive and slick cutting edge visualization portals, and increasingly challenging genomic databases. Clinical bioinformatics group is revolutionizing the health level exchange systems to integrate genomic and biomedical systems. We are looking for a talented and self-driven bioinformatics software engineer to help us to continue being the pioneer next generation sequencing based clinical software systems. As a Bioinformatics Software Engineer, you will work in a highly collaborative environment, engineering bleeding edge clinical and research software systems that directly impact the patient care and will be responsible for building the next-generation informatics systems revolutionizing the cancer care and diagnosis. You will also participate in developing high throughput data processing, petabyte scale data management, microservices oriented RESTful APIs, genomic and analytic portals, department-wide messaging/queuing system, and socket-based TCP/IP servers. We believe that this is an exciting role for someone who has the right background to be apart of our dynamic team. We can provide you with the opportunity to make a difference with your career.You Are:- Capable of building strong customer relationships and delivering customer-centric products- Able to work effectively in a fast paced changing environment solving for complex problems, and consistently achieves results, even under tough situations- Adept at learning quickly, applying insights from past efforts to new situations.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.- Resilient in recovering from setbacks and skilled at finding detours around problems.You Will:- Take part in the developing cutting-edge software systems for clinical diagnostics and to support existing clinical bioinformatics software.- Design, develop, and extend/maintain clinical bioinformatics automation pipelines, and our petabyte scale data management system.- Develop and maintain reporting/review portals which host results (from petabyte scale data pipelines) and work with in-house developed and public cloud solutions, a versatile full-stack software engineer.- Implement and follow the best practices in software development, code versioning, software testing, and deployment. Takes part in technical discussions including but not limited to code reviews, and build/release management.- Develop/Maintain clinical bioinformatics databases using MySQL, and MongoDB. Willing to learn and implement efficient database design methodologies.- Work with UNIX systems administrator to configure new and existing software packages for security, performance and maintainability.- Develop and maintains software systems that interface with other departmental and/or institutional systems through RESTful APIs.- Participate in design, development, and testing of additional internal and/or department-wide informatics systems.You Have:- Bachelor’s Degree with 4-6 years of software engineering experience. Master’s Degree with 2-4 years of experience preferred.- Experience with full stack web development especially with Python/Java/Ruby, Flask/Spring/Django, MySQL/MongoDB/GraphDB, React/Angular/Node.js/JavaScript is required.- Next generation sequencing and cancer genetics experience preferred but not required.- Experience with building front end data visualization portals, high volume data processing, messaging queues, and enterprise search engines is desirableBenefits:- Paid time off including vacation, bereavement, sick leave- Paid Parental Leave- Comprehensive medical, dental & vision, FSA and dependent care- Life Insurance and Disability Benefits- Fitness Discounts- 403(b) retirement savings plan match- Tuition Reimbursement- Commuter spending account #LI-POST
Are you passionate about collaborating with a team of clinicians and scientists at Memorial Sloan Kettering Cancer Center? Then join us here at MSK, where we can provide you with the opportunity to make a difference with your career. We believe that this is an exciting role for someone who has the right background to be a part of our dynamic team and who wants to apply their skills to support our mission here. We are looking for a Data Engineer to develop and support software applications, tools and data management pipelines for research and clinical purposes within the field of Digital and Computational Pathology. You will assist in the design, implementation and maintenance of tools that extract and manipulate data from various sources, including in-house and external databases, for use in the research and development of Computational Pathology tools and algorithms.You Are- A problem solver with the ability to think outside of the box, to find novel solutions to obstacles and setbacks.- A teammate with the ability to work well both independently and within a diverse team.- Hard working and passionate, believing strongly in our mission statement and goals.- Detail and deadline oriented, with the ability to proofread, thoroughly test, and submit high quality work on time.- An effective communicator with strong interpersonal skills.- Willing to learn new skills and adaptable to fluctuating workloads and deadlines.You Will- Create software and data pipelines that enable the ingestion, transformation and transfer of large quantities of structured and unstructured clinical data from various databases and filesystems sources, that are destined for the development of computation pathology applications and algorithms.- Build database logic to automatically fetch and store data in various forms.- Be responsible for server, application, and database development and the building and testing of high-performance, complex systems.- Produce required functional, technical, and user documentation (e.g., business requirements, functional and technical specifications, system architecture, data flows, end-users training requirements) on assigned projects.- Work and collaborate with scientists, engineers, IT operations and medical doctors to build tools manipulating data in order to build a new generation of artificial intelligence applications for cancer detection and treatment.- Learn the Pathology Department’s laboratory and diagnostic procedures as they pertain to the generation and flow of data in Digital and Computational Pathology.- Provide consultation and guidance to scientists, engineers, as well as other bioinformatics engineers and medical doctors, at the Center and partnering institutions.- Maintain and improve professional growth and development through participation in scientific and technical discussions, workshops, and seminars to keep current in the development of industry-grade software.You Need- Bachelor’s degree in Computer Science, Information Systems, Biomedical Engineering or related field- 4+ years of industry experience as a Data Engineer- Extensive experience in Python programming, or related language.- Extensive experience in the development of SQL database schema and query logic.- Experience with data warehouse architecture for large quantities of structured and unstructured data.- Experience with the design, detailed testing, and documentation of complex systems.- Experience with version control standard methodologies.Bonus- Experience with modern DevOps practices & technologies (e.g. Docker, Jenkins)- Experience with design and architecture of Data Lakes- Experience with design and architecture of NoSQL databases (e.g. Redis, MongoDB).- Experience with image processing software and techniques (e.g. OpenCV) and familiarity with image file formats#LI-POST
The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Regulatory Associate. As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Regulatory Associate is responsible for providing support to the Clinical Operations team for multi-center clinical trial activities from concept to close-out. Dedication to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role. This is an excellent opportunity to become part of an engaging and growing clinical research team.You will:- Partner with Project Associates to maintain comprehensive, GCP/FDA compliant, regulatory files for protocols.- Support Quality Control through support of the PCCTC monitoring program.- Perform regular audits to ensure that regulatory documentation is complete, up-to-date, and accurate and to ensure that the TMF is in compliance with regulatory agency requirements. Perform audits to ensure site qualifications are maintained throughout the duration of a study. - Prepare for internal and external audits of a protocol (e.g. conduct pre-audit review of the regulatory files).- Perform a complete Quality Assurance review of all regulatory documents in line with plans to close sites and/or studies.- Manage the PCCTC electronic TMF system, including system user management and system functionality assessment, implementation, and oversight. Support program-level TMF structure development and management and study-specific TMF setup. - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the conduct of a clinical study.- Complete all required certifications per company requirements (e.g., Human Subjects Protection, HIPAA), and ensure research team compliance of such trainings for all involved in the clinical trial. You need:- A bachelor's degree and 2-4 years of relevant clinical research experience or a High School Diploma with at least 4-7 years clinical research experience.- Working knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection.- Comfortable working in a dynamic environment.- Strong organizational, prioritization, and project management skills.- Strong computing skills including proficiency in MS Office products.- Excellent social, verbal and written communication skills.- Ability to tackle problems by using a logical, systematic, sequential approach.More information about the PCCTC:The Prostate Cancer Clinical Trials Consortium (PCCTC) was initiated in 2005 by the Prostate Cancer Foundation (PCF) and the U.S. Department of Defense (DOD) Prostate Cancer Research Program (PCRP) in response to critically unmet needs in prostate cancer clinical research identified by physician investigators and patient advocates. Established as an independent entity in 2014, the PCCTC, LLC is now the nation’s best-in-class multicenter Clinical Research Organization (CRO) specializing in ground breaking prostate cancer research. The PCCTC works together with distinguished investigators on a single mission: to design, implement and complete hypothesis-driven early phase trials in prostate cancer, translating scientific discoveries to improved standards of care. To fulfill its mission, the PCCTC developed a rare infrastructure, which has nurtured a culture of clear project co-development between investigators, research sites and industry partners.
Are you passionate about technology and playing a key role in redefining the future of cancer care? Join MSK’s API Platform team as we meet the challenge of cancer care as it defines a new model of care in the digital age. The API Platform team will enable our toolmakers to meet this challenge. The candidate will be manage our day to day operations of the API Platform which includes API Connect, App Connect and KAFKA Event Streams.The candidate should also have a good understanding of API Lifecycle management as we take it from design, creation, management, versioning, deprecation and retirement. The API Platform Engineer will help enable MSK to execute on its vision for leading cancer care in the new digital age. Are you up for the challenge? What you'll do: - Install, maintain and support the API Management Platform which include IBM API Connect, IBM App Connect, KAFKA Event Stream in multi-cloud environment.- Develop and document test plans for the Kubernetes and/or OpenShift infrastructure- Create automation scripts for promotion of APIs as it moves from Dev, Stage, QA and Production.- Build and publish APIs using IBM API Connect and design the logical topologies that include catalogues, spaces, plans and products.- Collaborates in an agile team with API Developers, Architects and Engineers.Who you are: - Experience with Unix/Linux administration in a large-scale environment with advanced skills in bash and/or python scripting.- Experience with tools such as Ansible Tower and Ansible playbook creation. Experience with application build automation with tools like Jenkins and Git.- Well-versed in API Security and different authentication models including SAML, OAuth 2.0 & OIDC.- Hands on experience with XML, YAML, XSLT, JSON and Swagger Definition files.- Experience in AWS or Azure Cloud development & deployment models and architecture with CI/CD exposure.- Experience using different scripting languages and comfortable working in both Linux & Windows OS systems.- Bachelor’s Degree LocationNYC - Midtown East near Grand Central BenefitsCompetitive compensation packages | Generous Vacation, Sick time + 12 holidays to recharge & refuel | Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care | 403b retirement savings plan match | Tuition Reimbursement | 12 Weeks Maternity/Paternity & Adoption Assistance | Commuter Spending Account | Fitness Discounts & Wellness Program | Resource Networks | Life Insurance & Disability | Remote Flexibility We believe in communication, transparency, and thinking beyond your 8-hour day @ MSK. It’s important to us that you have a sense of impact, community, work/life balance and personal well-being to be and feel your best. Our Hiring ProcessYou read the ad, agree it sounds like a great fit & apply -> Talent Acquisition contacts you to schedule a phone interview if your profile aligns and/or start the process with a tech assessment, max 45 min online -> after speaking with the Talent Acquisition Specialist, you will connect with the Hiring Manager by phone or video call -> if your experience is a fit, you will move forward to an on-site visit with the team -> post-interview feedback -> ideally an offer! -> reference check & onboarding -> orientation & official welcome to MSK #LI-POST
Clinical Nurse –Surgical Office Practice, GI Oncology (Outpatient NYC)Hours: 4 x 10 hour days, Monday–Friday, 8am - 6pm We are:- Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment- Nursing at MSK You are:- Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- A good decision-maker, with proven success at making timely decisions that maintains high standards of nursing care within the organization.- Actively seeking new ways to grow and be challenged, using both formal and informal development.- Approachable and comfortable with diverse groups of people and able to make others comfortable with you.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.- Capable of building strong customer relationships and delivering customer-centric solutions. You will:- Participate in a multidisciplinary team approach providing continuity of care for patients diagnosed with GI diseases. - Function in collaborative Nurse-Physician based Outpatient Care Delivery Model.- Provide comprehensive outpatient oncology care to patients and their caregivers.- Perform patient assessments; provide education and psychosocial support to patients and their caregivers.- Participate in coordinating oncology care for patients throughout the care continuum.- Participate in an individualized training/orientation program geared to providing nursing care in ambulatory setting. You need:- New York State RN license and BSN- 1. 5 years of related Medical Surgical experience required- 1. 5 – 2 years of oncology experience strongly preferred- Ambulatory care experience preferred- BCLS
The Grants and Contracts group of the Office of Research and Project Administration (ORPA) is seeking a confident and motivated Research Development Manager to join their team. Are you passionate about uncovering exciting funding opportunities for your investigators? Does your faculty consider you the ‘Grant Guru’ and seek your guidance with grant submissions? Are you someone who loves to develop strategies? Are you energized by presenting information to stakeholders and educating the research community about grants? If you answered yes to these questions, this position might be for you. Our Grants and Contracts group leads the pre-award administration of research grants and contracts funded by federal, state, and private agencies. As the Research Development Manager, you will:- Develop positive relationships with MSK investigators and researchers, and identify and prospect exciting funding opportunities on their behalf.- Cultivate effective grants submission strategies that lead to successful awards. - Partner with faculty and research teams to identify unique funding sources.- Engage in proposal development activities, interpret and explain funding agency and institutional requirements, and provide review and editing assistance, as well as training and outreach to the Center community.You are:- An authority on pre-award grant submission process. - Eager to understand what interests and drives your client investigators and seek opportunities that are a match.- Self-motivated, willing to take action with demonstrated ability to establish relationships, prioritize and multi-task on parallel projects- Seen as the “go-to” person and easily gain the trust and respect of your client group.- Able to adapt to ambiguous situations and produce results.- An effective communicator, capable of resolving how best to reach different audiences and executing communications based on that understanding. - Effective at gaining the support and dedication of others by engaging them around your opinion and priorities.You have:- A Bachelor’s degree in the biological sciences or similar fields, Master's degree preferred. - At least 5 years experience in a research administration office, preferably in basic and translational research.- Ability to independently apply a broad range of technical and specialized knowledge and significant job-related experience to handle complex work assignments.- Experience with the development/submission of research grants, and with reading and interpreting funding opportunities. #LI-POST
Research Financial Management is a part of the Research and Technology Management Division, and is responsible for post-award grant administration, including the comprehensive financial management of MSK's organized research support. The department is staffed by trained research administrators who possess a strong background in and knowledge of the financial, administrative, and compliance guidelines of the Federal government, as well as that of the various external sponsors that provide financial support to Sloan-Kettering Institute. The Research Financial Management team is currently seeking a Research Financial Manager (Sponsored Projects) to join their team. The RFM is responsible for managing and administering all activities associated with awarded grants and contracts. The Research Financial Manager serves as the principal administrative resource and contact between investigators, external funding agencies, and MSK, and acts as an information consultant for the researchers in the institution.This position also manages post-award financial activities, including review and approval of fiscal expenditures, the application, and analysis of budgetary controls for funding sponsors, as well as ensuring institutional compliance with federal, state, agency and other applicable governing regulations, policies and procedures concerning sponsored and non-sponsored research. You Will: - Assume financial control of assigned departments and review funding expenditures by the investigators for the cost allowability, administrative reasonableness, appropriate award allocability and funding availability.- Establish management and administrative controls for all grants, contracts and other research funding mechanisms, and advise investigators and department administration about funding availability and potential issues arising from either deficient or surplus award funding.- Ensure rules for grants management, including those regulating federal sources, voluntary agencies, industrial contracts, philanthropic sources and MSK institutional policy are understood, disseminated and complied with.- In collaboration with the investigator, establish and maintain annual budgets for research awards.- Act as a resource for research investigators in the area of financial award management, and as a point of contact between the investigator and the awarding agencies.- Explain funding issues to awarding agencies, collaborating institutions, and internal MSKCC departments.- Maintain discretion for confidential information and appropriately handle critical information and sensitive situations.- Collaborate with Office of Research and Project Administration (ORPA) units and RTM departments to provide comprehensive information and service to investigators and department administration.- Interact with all levels of staff and external contacts and work under pressure while maintaining a professional demeanor.You Are: - An effective communicator; with strong interpersonal and oral communication skills and the ability to effectively interact with designated faculty and administrations, as well as with external contacts.- Self-motivated; with a high level of ability to work with minimum supervision.- Collaborative and comfortable working as part of a team to interpret policies and procedures.- Solution oriented and able to exercise sound judgment to solve problems within the scope of the position.- A multi-tasker capable of managing your designated workload while providing quality service and meeting deadlines through organization, interpersonal skills and accurate prioritization of activities.- Accurate in developing and managing budgets, projecting expenditures and managing recommended solutions.- Flexible to shifting priorities.You Have: - A minimum of a Bachelor's Degree OR 5+ years of experience directly related to the responsibilities of the role.- At least 2-4 years of experience in a related field; preferably an administration environment performing duties similar to the above.- Knowledge of federal agency regulations, policies and procedures, circulars, laws and federal acquisition regulations applicable to sponsored programs.- Computer aptitude, including word processing and spreadsheet development.- Knowledge of standard administrative procedures and office equipment. #LI-POST
We are seeking a Research Project Associate for our Multicenter Research Team.You Will:- Serve as the MSK point of contact for external sites in activities related to the clinical trial and maintain real-time knowledge of all aspects of the trial, including data management, subject management and regulatory oversight. - Ensure that participants are treated in accordance with the protocols and that study conduct is in accordance with the CR protocol and applicable policies and regulations.- Conduct eligibility verification of external participants enrolled in MSK clinical trials.- Conduct monitoring and auditing of MSK MCT IITs as directed by the Multicenter Manager; these assignments will include but not be limited to: protocol compliance, data verification, and regulatory compliance - Perform diverse administrative and research-related duties requiring analysis, good judgment, comprehensive understanding of all federal regulatory standards and ICH (International Center for Harmonization) mentorship on Good Clinical Practice (GCP) and MSK CRA SOPs. - Participate in internal/external clinical trial meetings to update the study team/external sites with relevant information related to the clinical trial. - Participate in special projects and task forces as determined by management.You are:- An excellent communicator. Able to receive and relay information accurately and effectively with strong written and verbal communication. - Capable of anticipating and stabilizing the needs of multiple partners.- Inventive, securing and deploying resources effectively and efficiently.- Adept at building partnerships and working reciprocally with others to meet shared objectives and goals.- Able to operate effectively, even when things are not clear or the way forward is not obvious.- Detail-oriented, able to multitask, and have excellent time management skills. - A self-starter/able to operationalize ideas and suggestions from research team.- Must be able to work independently as well as collaborate with others.You Have:- A High School Diploma/GED with 2-4 years of clinical research experience or equivalent required.- Bachelor’s degree preferred with experience in clinical research and/or other applicable research investigation. Relevant graduate work considered in lieu of minimum experience.Comprehensive knowledge and understanding of the regulations pertaining to human subject protection, Good Clinical Practice and other clinical research essential #LIPOST
The mission of CMO Computational Sciences (CCS) is to innovate new computational science that accelerates discovery in, and the practice of, molecular-driven cancer medicine. This team of experienced computational biologists catalyze institution-wide collaborative science in translational genomics. Projects focus on immunogenomics, correlative genomics in early-phase clinical trials, evolutionary analysis of disease, mutant allele discovery and validation, disease-specific and pan-cancer studies, precision disease model genomics, novel methods development, the interface of inherited and somatic genetics, the development of complex genetic signatures, and new prognostic and therapeutic biomarkers. You Are:- Capable of building strong customer relationships and delivering customer-centric solutions- A good decision-maker, with shown success at making timely decisions that keep the organization moving forward- Able to work effectively in an environment notable for complex, sometimes contradictory information- Consistently achieving results, even under tough circumstances- Adept at planning and prioritizing work to meet commitments aligned with organizational needs- Adept at building partnerships and working collaboratively with others to meet shared objectives and goals- An effective communicator, capable of resolving how best to reach different audiences and executing communications based on that understanding- Resilient in recovering from setbacks and skilled at finding detours around obstacles- Able to operate effectively, even when things are not clear or the way forward is not obvious- Adept at learning quickly, applying insights from past efforts to new situationsTo be considered for a Computational Biologist II, you need:- Masters of Science in cancer biology, genetics, computational biology, or a related discipline.- At least three years of experience in academic or corporate research.- Outstanding academic record.- Strong computational and programming skills, including thorough experience with the following: UNIX environment, next-generation sequencing analysis packages (e.g., Samtools, GATK), advanced programming skills, statistical packages.- Knowledge of bioinformatics concepts, methods, and tools.- Familiarity with genomic data, tools, and databases.- Ability to solve complex problems individually and as part of a team.- Strong organizational and troubleshooting abilities, attention to detail and accuracy, and outstanding oral and written English communication skills.To be considered for a Sr. Computational Biologist, you need:- Master’s, Ph.D., or equivalent in biological science, mathematics, physics, bioinformatics or related discipline with strong quantitative background. Proficiency with scientific computing software (Matlab, R) and scripting languages is required.- Solid programming skills and extensive research experience in the biological sciences. A thorough understanding and experience in statistics is strongly preferred.- Research experience in statistical genetics/genomics strongly preferred and a familiarity with next-generation sequence data and analysis tools is a plus.- Able to work independently and collaboratively; making necessary connections with experts in various biological and clinical groups.- Excellent oral and written English communication skills; experience in delivering oral scientific presentations and writing scientific articles strongly preferred.#LI-POST
We are seeking an experienced per diem Respiratory Therapist to render respiratory therapy to patients as ordered by a physician, physician assistant or nurse practitioner! You will also consult with other health care practitioners in the management or prevention of cardiopulmonary disorders.You are:- Able to problem solve operational, personnel, and patient issues- Highly motivated and able to motivate and work well with others; able to adapt to constantly changing environment- Someone who has excellent communication skills and who supports the open expression of diverse ideas and opinions- Someone who can follow through on commitments and who acts with a clear sense of ownership.- Team focused and collaborate with other disciplines in the coordination of patient care.You will:- Render respiratory therapy to patients as ordered by a physician, physician assistant, or nurse practitioner.- Consult with and aide other health care practitioners in management or prevention of cardiopulmonary disorders, with minimal supervision.- Assess patient’s condition and follow up to ensure appropriateness of therapy.- Instruct and participate in the orientation of new employees.- Educate patients and their families regarding respiratory treatment/therapy.- Assist in providing education to other disciplines regarding respiratory therapies and modalities.You have:- An Associate's Degree in Applied Science and Respiratory Therapy.- A current NY State Respiratory Therapist License.- Current NBRC Credential as a Registered Respiratory Therapist.- BLS required, ACLS preferred.- Preferably Pediatric/PICU experience.- Certification of fitness from the NYCFD preferred.Hours of work:- Shift may vary depending on the needs of the department (mainly in search of varied night positions)
We are a group of physicians and scientists in the Molecular Pharmacology Program at the Sloan Kettering Institute and Department of Pediatrics at the Memorial Sloan Kettering Cancer Center. We carry out research in cancer biology and pediatric oncology, and our current work is focused on the phenomenon of cellular plasticity, as it relates both to the fundamental mechanisms of cancer pathogenesis and emerging rational therapies. We are seeking a Lab Manager to join our team!In this position, you will lead and conduct laboratory activities including performing experiments and analyzing data, maintaining supply inventory and experimental apparatus, and working with other lab members.Duties and responsibilities:- Perform laboratory experiments, which may be moderate to complex with growing independence.- Record data and perform basic analyses using mathematical and statistical modeling.- Assist in the maintenance of mouse colonies.- Help to prepare presentations and written articles for publication.- Prepare laboratory reagents, chemicals, instruments, and maintain equipment.- Maintain supplies inventory in accordance with departmental procedures.You have:- Bachelor's degree in STEM- Minimum 3-years experience in a biological lab research- Ability to compose written correspondence and to present information in a clear, concise manner.- Ability to communicate, explain, interpret, share and present information- Ability to set priorities among several tasks simultaneously and meet established deadlines.- Ability to coordinate and maintain all research information- Proficiency in the Microsoft Suite- Hands-on experience with the breeding of genetically-engineered mice, mouse husbandry and procedures; mammalian tissue culture and procedures, and analytical experiments in molecular and cell biology.- Prior experience in laboratory management is a plus.Along with your resume, please submit a cover letter addressed to Dr. Alex Kentsis explaining your interest. NO APPLICATIONS WITHOUT A COVER LETTER WILL BE REVIEWED In your letter, please include: Specific questions you have about the lab that you would expect to learn by working here. Short-term and long-term career goals, how this position would advance them.Your accomplishments in your current position and reasons for seeking change. How you are prepared to excel in the specific responsibilities of this position. Please visit http://alexkentsis.net/prior to preparing your cover letter. #LI-POST
The Data Analyst is an integral member of the Office of Research and Project Administration (ORPA) team that is responsible for managing, analyzing and maintaining the integrity, completeness and accuracy of MSK's sponsored projects proposal and award data. You will develop and maintain production reports, and oversee grants management information systems and processes, in collaboration with Research and Technology Management's Information Technology Department. You will:- Analyze MSK’s grant data, ensure data integrity, and oversee data quality assurance.- Create high level ad hoc reports required or requested by ORPA and the MSK research community, including MSK's senior leadership, Vice Presidents and Board of Directors.- Use SQL, Tableau, Excel, Cognos Reports, Cognos Query Studio, and/or internal/external systems, websites and databases to design or produce reports for RTM or MSK research community use that serve to further educate and inform these constituencies about MSK research activity and productivity and improve workflow.- Serve as a liaison with RTM IT to determine optimal enhancements for current systems and workflow, and to develop tools to improve systems.- Design and lead test plans for system enhancements, and oversee rigorous testing of new software functions.- Responsible for creating and implementing training modules and presentations for all aspects of grants management information systems and processes for internal users and the MSK research community.- Ensure ORPA databases contain correct, compliant and necessary information; monitor data in the institutional grants management system for accuracy and completeness.- Utilize proposal, award and systems knowledge to analyze data and regularly scheduled reports and work flow, ensuring report integrity, quality control and completion.- Provide technical assistance with respect to data input, reports, reporting tools and grants management systems to MSK’s research communityYou are: - A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. - Adept at planning and prioritizing work to meet commitments aligned with organizational goals.- Willing to take action and eager to accept new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm. - An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding. - Adept at building partnerships and working collaboratively with others to meet shared objectives and goals. - Able to operate effectively, even when things are not clear or the way forward is not obvious. - Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. You need:- Bachelor’s Degree with 2-4 years of experience with data analysis.- Familiarity with relational databases, SQL, Tableau, and Excel.Preferred:- Prior experience working with sponsored research proposal and award #LI-POST
We have an exciting opportunity to join Clinical Research Administration (CRA) as an Operations Coordinator. This role offers you the opportunity to provide administrative leadership to the Vice President, Unit Leads and the Director of Operations and Finance. In addition, you will make recommendations to improve operations, divisional efficiencies and human resource processes. You will engage in special projects and working groups to improve administrative operations across all CRA. You will also oversee operations and activities of the administrative support staff across multiple locations. What will you do:• Provide guidance to managers on Workday transactions and ensure the dissemination of required information to new hires. • Communicate effectively with all levels of staff including administration, research and clerical support staff, and institutional leaders. • Collaborate with senior management to implement new processes and monitor/modify these changes to ensure success. • Provide backup facilities and emergency management coverage for the Administrative Coordinator. • Manage and maintain CRA’s personnel files, including assessments and mandatory learning documentation as well as administrative policies and procedures. • Oversee payroll for the CRA units. • Demonstrate excellent problem-solving skills to analyze situations, draw conclusions, make recommendations and convey this information in a timely and proficient manner. • Set priorities among several tasks simultaneously and meet established deadlines for multiple projects simultaneously. • Guide staff to ensure programmatic activities adhere to established time frames and deadlines. • Plan, organize, facilitate and lead meetings. Who are you:• Bachelor’s degree is required. • 2-4 years of administrative work experience • Minimum of 2 years supervisory experience. • Excellent oral and written communication skills. • Project management experience and MSK experience is highly preferred. • Intermediate to advanced SharePoint and MS Office skills Location: NYC - Midtown East near Grand Central Benefits:Competitive compensation packages | Sick Time | Generous Vacation + 12 holidays to recharge & refuel | Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care | 403b retirement savings plan match | Tuition Reimbursement | Parental Leave & Adoption Assistance | Commuter Spending Account | Fitness Discounts & Wellness Program | Resource Networks | Life Insurance & Disability | Remote Flexibility We believe in communication, transparency, and thinking beyond your 8-hour day @ MSK. It’s important to us that you have a sense of impact, community, and work/life balance to be and feel your best. Our Hiring ProcessYou read the ad, agree it sounds like a great fit & apply -> Talent Acquisition contacts you to schedule a phone interview (if your profile aligns) and/or start the process with a tech assessment, max 1 hr online -> after speaking with the Talent Acquisition Specialist, you will connect with the Hiring Manager by phone or video call -> if your experience is a fit, you will move forward to an on-site visit with the team -> post interview feedback -> ideally an offer! -> reference check & onboarding -> orientation & official welcome to MSK. #LI-POST
