Career Opportunities

 

Here are our current open positions. To learn more about the role and apply, click on the job title.

Use this form to perform another job search

The system cannot access your location for 1 of 2 reasons:
  1. Permission to access your location has been denied. Please reload the page and allow the browser to access your location information.
  2. Your location information has yet to be received. Please wait a moment then hit [Search] again.
Click column header to sort

Search Results Page 5 of 5

Job Locations USA-NY-New York
Posted Date 2 months ago(5/18/2020 5:26 PM)
The Financial Planning Department at MSK is seeking a Financial and Research Analysis Specialist to join their growing team.As the Financial and Research Analysis Specialist, you will:- Be responsible for supporting three key Financial Planning functions including the annual Operating & Capital Budget, the Cash Flow Model, and Inter-corporate cost allocations. - Provide support and guidance to Strata stakeholders across the enterprise during the Budget development period, provide supporting analytics to the Cash Flow Model and help build and maintain inter-corporate cost allocations used extensively in the audit of the Financial Statements, Indirect Cost Proposal, and Medicare and NY State cost reports. - Work closely with the Senior V.P. Financial Planning, Director – Cost & Budgets, and key budget stakeholders across the Center and Hospital divisions. - Provide a vast amount of support to the Strata Systems Group including providing coverage to the Help Desk during the time the budget tool is available to clinical and administrative stakeholders. - Perform ad hoc financial analyses as needed on a number of special projects and inquiries from the Executive Leadership teams across the enterprise.You are:- A good decision-maker, with shown success at making timely decisions that keep the organization moving forward.- Able to operate optimally, even when things are not clear or the way forward is not.- Willing to take action and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- Adept at creating partnerships and working collaboratively with others to meet shared objectives and goals.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.You have:- A Bachelor’s Degree and a minimum of 2 years working in a similar position/environment, or at least 6 years of relevant experience in lieu of a Bachelor's Degree.- Proven knowledge of Microsoft applications (Access and Excel).- 1-3 years of Strata & IBM TM1 experience preferred.- Knowledge and experience in budgeting and forecasting.- Corporate allocation experience essential.Please note: Candidates seeking an accounting-related position should consider other opportunities.#LI-POST
Requisition ID
2020-42418
Category
Professional - Finance
Job Locations USA-NY-New York
Posted Date 2 months ago(5/13/2020 3:56 PM)
MSK’s Development Operations team is seeking a passionate, strategic, organized, and highly motivated Project Manager to join its growing team. The Project Manager will analyze, initiate, and drive projects through to successful completion, provide status updates, and make recommendations to Senior Leadership in Development.We are:The Development Operations team is responsible for the technical infrastructure and business operations that support the Development Department. We aim to increase MSK’s fundraising potential through the creation of innovative technology and process solutions.You will:As assigned, initiates, plans, develops and conducts project methodologies to facilitate departmental initiatives and fulfill programmatic needs.Performance Expectations:- First point of contact for projects and assignments- Participates in the development/timeline and facilitates business and action plans to progress departmental initiatives- Develops and sustains project work flows and timelines- Leads ongoing projects and monitors issues and progress- Works closely with leadership and Development staff to plan and implement software development- Serves as a thought partner in the development of solutions and new initiatives- Serves as primary liaison for appropriate contacts both within the institution and with vendor partners- Engages in the direction of the project, recommends, and directs new and modified action plans- Understands external regulations as well as MSK policies and procedures and is able to interpret their implications for the project- Implements standard operating procedures for project management across the Development organizationYou 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 goals- 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 situationsYou have:- A Bachelor’s degree or at least 8 years of relevant experience in lieu of a Bachelor's degree- 4-7 years of Project Management related experiencePreferred:- PMP Certification- A Master’s Degree in Business Administration or related field- Experience with Blackbaud CRM or other CRM systems- Experience with Jira and Confluence- IT project management experience#LI-POST
Requisition ID
2020-42293
Category
Professional - Development
Job Locations USA-NY-New York
Posted Date 2 months ago(5/12/2020 11:49 AM)
Memorial Sloan Kettering Cancer Center is seeking Radiation Therapists for our main campus site in New York City.  Memorial Sloan Kettering’s Department of Radiation Oncology is dedicated to providing superior care to our patients while leading innovations in clinical, translational, and laboratory-based research. Our experts helped pioneer techniques such as intensity-modulated radiation therapy and are world leaders in their subspecialties, including brachytherapy, stereotactic radiosurgery, and palliative approaches. We are looking for a dedicated and passionate team player to join the NYC team. You Are:  - A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. - Adept at building partnerships and working collaboratively with others to meet shared objectives and goals.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.You Will:- Administer radiation oncology treatments according to the Radiation Oncologist's prescription under a minimum of supervision.- Keep accurate daily records of treatments administered.- Teach students technical procedures during their clinical rotations under the supervision of the Chief Therapist.You Have:- Graduate of an A.M.A. approved 2-year training program in radiation therapy technology or its equivalent is required.- Registered Radiation Therapy licensure in the state of New York is required.- Certification in American Registry of Radiologic Technology (ARRT) is required. #- Minimum of 2 years of experience as a staff radiation therapist strongly preferred.   
Requisition ID
2019-36625
Category
Allied Health - Medical Physics and Radiation Therapy
Job Locations USA-NY-New York
Posted Date 2 months ago(5/12/2020 8:53 AM)
  https://youtu.be/9R7QoNfmm0w Consider an outstanding opportunity to be at the forefront of supporting Memorial Sloan Kettering Cancer Center's renowned leadership. We have an exciting opportunity in our Thoracic Surgery Service as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA) coordinates and maintains the assigned research portfolios for a Service and/or Department.Memorial Sloan Kettering physicians conduct one of the world’s largest clinical cancer research programs. Investigators from various fields and departments join efforts to improve the prevention, The faculty and staff of Memorial Sloan Kettering’s clinical departments and divisions possess an unparalleled depth and breadth of clinical expertise. Our outstanding scientists and clinicians work together to drive innovation and seek some of the greatest challenges of biomedical science. You Will:- Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols.- Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight.- Effectively communicate the overall study progress to various internal and/or external partners, and identify study trends and build/implement solutions.- Perform diverse research-related functions using sound judgment and exceptional interpersonal skills.You are:- Adept at anticipating and prioritizing work to meet commitments of multiple partners.- Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals.- Known as someone who improves processes and proactively, independently identifies solutions that anticipate partner needs.You have:- HS Diploma/GED with 2-4 years meaningful work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelor’s Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory.- Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required.- Proficiency with the Electronic Medical Record (EMR) system.- Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics.- Knowledge of clinical research data collection processes in accordance with GCP. 
Requisition ID
2020-42202
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 2 months ago(4/28/2020 9:29 PM)
At MSK, we’re running one of the largest clinical trials programs for cancer in the country. In the Department of Pediatrics, we are dedicated to developing safer and more-effective therapies to control and cure childhood cancers so our patients can return to their daily activities as quickly as possible. We are seeking a Clinical Research Manager (CRM) for the Solid Tumor I service. The CRM serves as an integral member of the research team and will Implement standard for research protocol management, policies and  procedures to ensure the highest quality management of clinical research studies.  As a CRM, you will be responsible for the following:- Staff Management: You will supervise the training/development and performance management for a large number of direct and indirect reports throughout the service.- Protocol Development: Lead aspects of the protocol development process including but not limited to preparing protocols, consent and other essential study document review.- Financial Management: Work closely with the appropriate partners, forecast trial resource needs, and assess staffing resource needs for program and senior leadership to ensure appropriate line function allocations.- Clinical Trial Reporting: Generate protocol portfolio status reports for key partners. Implement solutions for streamlining and accelerating the monitoring and review of clinical trials to significantly increase accrual to clinical trials, data cleaning, data quality, and trial completion.- Quality Assurance: Participate and ensure preparedness in routine audits for data quality, regulatory compliance, patient safety issues related to clinical trial. Communicate and ensure compliance with company policies and procedures, quality standards and improvement initiatives.You Are:- Effective at building formal and informal networks inside and outside the organization to further departmental and institutional goals.- Adept at building partnerships and working collaboratively with others to meet shared objectives and goals.- A good decision-maker, with shown success at making timely decisions that keep projects on deadline.- Detailed oriented and able to multi task.- Able to manage competing priorities.- Eager to foster talent and mentor staff in their current roles and develop them so that they can attain the next steps in their career.You Have:- A Bachelor's degree (prefererd) with at least 4 years of clinical research experience.- 2+ years of staff management experience.- Thorough knowledge of Good Clinical Practice (GCP) guidelines, Human Subject Protection, clinical trial design, regulatory processes, and clinical development process required.- Effective written/verbal communication and oral presentation skills required. Excellent interpersonal, leadership, decision-making and issue resolution skills are essential. #LIPOST
Requisition ID
2020-41768
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 3 months ago(4/13/2020 5:14 PM)
We are seeking a Clinical Research Manager (CRM) for the following teams in the Department of Medicine. Breast MedicineSolid Tumor INeurology   The CRM serves as an integral member of the research team and will own the daily operations and activities of the program. This is an excellent leadership opportunity within our growing clinical research team. The CRM will be responsible for the following:- Staff Management: You will supervise the training/development and performance management for a large number of direct and indirect reports throughout the service.- Protocol Development: Lead aspects of the protocol development process including but not limited to preparing protocols, consent and other essential study document review.- Financial Management: Work closely with the appropriate partners, forecast trial resource needs, and assess staffing resource needs for program and senior leadership to ensure appropriate line function allocations- Clinical Trial Reporting: Generate protocol portfolio status reports for key partners. Implement solutions for streamlining and accelerating the monitoring and review of clinical trials to significantly increase accrual to clinical trials, data cleaning, data quality, and trial completion.- Quality Assurance: Participate and ensure preparedness in routine audits for data quality, regulatory compliance, patient safety issues related to clinical trial. Communicate and ensure compliance with company policies and procedures, quality standards and improvement initiatives.You need:- At least 4 years of clinical research experience.- 2 years or more of direct staff management experience.- Thorough knowledge of Good Clinical Practice (GCP) guidelines, Human Subject Protection, clinical trial design, regulatory processes, and clinical development process required.- Therapeutic and Oncology Research experience strongly preferred.Effective written/verbal communication and oal presentation skills required. Excellent interpersonal, leadership, decision-making and issue resolution skills are essential. #LI-POST 
Requisition ID
2020-41452
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 3 months ago(4/3/2020 2:32 PM)
At MSK, we’re running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We are seeking a Research Regulatory Associate (RRA) to join our Genitourinary Non-Prostate (GUNP) service within the Department of Medicine. In this role, you will ensure the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will:- Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development.- Assist in protocol submission, drafting of consents, reviewing protocol logistics.- Assist in audits- reviewing and collecting regulatory documents.- House all CVs, medical licenses, certifications and ensure they are current.- Participate in special projects and task forces as determined by management.- Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol.- Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed.- Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff).- Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. - Ensure that research protocols are approved by the Institutional Review Board and followed as written.- Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met.- Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested.- Provide leadership, organizational, creative, or clerical support to established and new research initiatives.You Are:- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. - Able to hold yourself and others accountable in order to achieve goals and live up to commitments.- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. - Knowledgeable 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).You Have:- A minimum of a High School Diploma with experience in clinical research or applicable experience.- Bachelor’s degree is preferred.- At least 1 year of experience working in clinical research, preferably with experience in the regulatory space, is required. Note:  There will be some weekend work expectations to cover potential Serious Adverse Events (SAE) reporting.
Requisition ID
2019-35359
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 3 months ago(4/2/2020 7:14 PM)
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.
Requisition ID
2019-38217
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 3 months ago(3/24/2020 3:24 PM)
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
Requisition ID
2019-36980
Category
Information Technology
Job Locations USA-NY-New York
Posted Date 4 months ago(3/12/2020 12:33 PM)
We are looking for highly motivated postdoctoral fellows interested in investigating immune spatial heterogeneity in human cancers.  These projects are based on high-dimensional tissue imaging of the tumor and associated microenvironment with single-cell protein expression analysis and subsequent integration of genomic DNA/RNA profiling.  The intention is to better define the function and development of the tumor/immune ecosystem to ultimately improve patient immunotherapeutic selection and prognostication, to better understand and overcome therapeutic resistance and to improve our understanding of biologic states in space and time.In this role you will: - Collaborate with quantitative experimentalists and computational scientists to conduct and publish research in a rapidly expanding investigational field with significant room for growth and ground-level development- Use new experimental tools and design novel methods and assays to address problems in human tumor immunology- Design and actualize high-dimensional spatial profiling studies within the immunopathology lab- Work with high dimensional imaging data from a variety of cutting-edge platforms such as MIBI, Codex, Vectra/Polaris and Nanostring GeoMx- Design strategies to analyze high dimensional imaging data- Integrate imaging data with genomic DNA/RNA profiling- Correlate findings with ongoing and recent clinical trials outcomes- Author journal papers and attend conferencesThe ideal candidate should have: - PhD or MS degree in immunology- Publication record in biologic or quantitative sciences- Experience with R for data analysis and statistics- Coding skills (esp. Python) would be helpful- Recent graduates, MS, and PhD candidates who will defend soon are welcomeInterested applicants should apply including CV, a letter outlining your interest and names/contact infomraiton of three references.  
Requisition ID
2020-41021
Category
Faculty – Pathology
Job Locations USA-NY-New York
Posted Date 4 months ago(3/6/2020 1:18 PM)
We Are:Research is integral to our mission at Memorial Sloan Kettering, and clinical trials help us discover better forms of patient care and treatment. Our extraordinary scientists and clinicians work together to drive innovation and tackle some of the greatest challenges of biomedical science.We are seeking a Clinical Research Specialist for the Department of Medicine-GYN-Biospecimen, focusing on responsibilities related to the coordination of clinic. In this role, you may be assigned working in the clinic, preceptorship of research staff, and special assignments (i.e. short-term studies, CRC training, etc).You Are:- Curious and eager to take on a wide variety of problems across the clinical research community at MSK- Adaptable to the demands of other internal groups- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward- Consistently achieving results, even under tough circumstances- Able to hold yourself and others accountable to achieve goals and live up to obligations- 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 obstacles- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances within the various departmentsYou Will:- Be responsible for coordinating and performing tasks in clinic- Provide clinic support by assisting with patient management on study- Support and help ensure complete regulatory compliance and data collection in clinic- Coordinate meetings with the PIs and provide assistance to other CRCs as needed- Ensure that all appropriate institutional, state, and federal regulations are followed throughout the research protocols- Assist with training new staff members as needed- Assist with short-term projects and provide cross-coverage to various research teamsYou Have:- A Bachelor’s degree plus one year of clinical research experience, or in lieu of a Bachelor's degree - a high school diploma with 3 years of clinical research experience- Excellent problem-solving abilities to analyze situations, draw conclusions, make recommendations as needed and convey this information in a timely and proficient manner- The ability to multitask and use specialized knowledge and experience to handle complex work assignments, including cross-coverage throughout the institution- A dedication to attention to detail and a natural inclination to take initiative
Requisition ID
2019-36714
Category
Research - Other
Job Locations USA-NY-New York
Posted Date 4 months ago(3/3/2020 1:33 PM)
The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Correlative Science Associate (CSA). As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Correlative Science Associate is responsible for supporting the Correlative Science Manager in the oversight of all studies related to collection, processing, and correlation of biomarkers with clinical and patient reported outcomes. The Correlative Science Associate will be expected to work with the Clinical Data Management and Clinical Operations teams to manage multi-center clinical trial activities by providing correlative expertise. Commitment to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role.You will: - Manage complex correlative registries and non-therapeutic trials as well as correlative studies included within multi-institutional therapeutic clinical trials across a diverse research portfolio.- Assist in designing clinical trials including correlative and translational design and manuals, protocol and informed consent drafting, safety and regulatory document drafting, etc.- Communicate effectively and establish strong working relationships with a diverse matrix of clinical trial sites, investigators, pharmaceutical & biotechnology partners, and other important stakeholders.- Synthesize complex correlative clinical trial information into actionable plans.- Provide necessary documentation in compliance with existing standard operating procedures, regulatory guidelines, etc.- Assist in maintaining necessary clinical trial conduct documentation - Communicate and work effectively with all stakeholders You need: - High School Diploma/GED with at least 4 - 7 years relevant clinical research, laboratory and/or medical/science experience OR a Bachelor's degree in STEM with 2 years of clinical research, laboratory or medical/science experience OR a Master’s degree in a scientific or medical discipline with clinical research, laboratory and/or medical/science experience.- Strong background knowledge of translational research and correlative science in relation to oncology. - Experience working with biospecimen collection and processing and/or biomarker analysis is a plus. - Ability to manage clinical research projects with strict deadlines.- Knowledge and experience with clinical trial execution.- Working knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection.- Knowledge of clinical trial regulatory and safety management preferred.- Comfortable working in a fast-paced environment.- Strong organizational, prioritization, and project management skills.- Strong computing skills including proficiency in MS Office products.- Excellent interpersonal, verbal and written communication skills.- Ability to solve problems by using a logical, systematic, sequential approach.Experience working with prostate cancer clinical trials is a plus. #LIPOST 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 premier multicenter Clinical Research Organization (CRO) specializing in cutting-edge 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 unique infrastructure, which has fostered a culture of transparent project co-development between investigators, research sites and industry partners. 
Requisition ID
2020-40593
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 4 months ago(2/28/2020 10:37 AM)
Memorial Sloan Kettering Cancer Center is looking for a highly motivated Histology Research Scientist to join the Automated Histology Group of the Molecular Cytology Core Facility, Sloan Kettering Institute, MSKCC.  The Histology Research Scientist will work with the core team and directly with users. Recent technological advances have increased the complexity and sophistication in setting up successful experiments for the detection of proteins and RNAs in situ in cells, tissues, and organs. Thus, in order to run successful experiments, an understanding and preserving the architecture and natural characteristics of biological samples is required, as well as identifying quality reagents, developing and executing specifically tailored machine-based protocols. In partnership with the Core Team and the researchers will prepare reports, manuscripts, and proposals for new instrumentation. This individual will report to the Molecular Cytology Core Head.  Key Responsibilities Include: - Learn, operate, and expand the technologies available at the core facility.- Perform evaluation and integration of new multiplex technologies for precise multiplex spatial detections.- Involved in discussions and collaboration with the users on strategies for proper sample preparation and antibody validations to identify the best.- Assist in lab organization and record-keeping, primary management of equipment, supplies, user training, scheduling, and billing at the core facility.- You will have the opportunity to identify additional responsibilities that match your interests, such as organizing and teaching classes and workshops, organizing discussion groups/journal clubs, developing protocols for testing reagents and equipment performance.- Establish contact with basic and clinical researchers from the US and all over the world, paving the way for successful professional growth. Qualifications:- Ph.D. degree- Strong desire to establish a career in a core facility - The ability to communicate effectively in verbal and written form with users and core staff is essential- Experience in histology, biochemistry, and immunology - Experience with automated staining platforms is a plus - Desire to explore and implement innovative spatial multiplex technology - Excellent written and verbal communication skills and experience with Excel, PowerPoint, Photoshop 
Requisition ID
2020-39632
Category
Research - Laboratory
Job Locations USA-NY-New York
Posted Date 4 months ago(2/24/2020 11:46 AM)
 Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education.  We have an exciting opportunity in our Early Drug Development Service as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA) coordinates and maintains the assigned research portfolio for a Service and/or Department.You Will:- Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols. - Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight. - Effectively communicate the overall study progress to various internal and/or external stakeholders, and identify study trends and create/implement solutions. - Perform diverse research-related functions using sound judgment and exceptional organizational skills.You are:- Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders.- Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals.- Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs.You have:- HS Diploma/GED with 2-4 years relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelor’s Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory.- Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required.- Proficiency with the Electronic Medical Record (EMR) system.- Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics.- Knowledge of clinical research data collection processes in accordance with GCP.
Requisition ID
2020-40257
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 5 months ago(2/6/2020 3:01 PM)
A senior research scientist position is available at Memorial Sloan Kettering Cancer Center for highly motivated candidates with a wide experience in molecular and cellular biology applied to cancer research. The laboratory headed by Dr. Andrew Kung, located in the Mortimer B. Zuckerman Research Center, focuses on translational research with the overarching goal of credentialing new therapeutic targets, identifying molecular biomarkers of response, and validating targeted therapeutic strategies for pediatric malignancies. The ideal candidate should have: - High proficiency in a variety of molecular and cellular biology techniques- Strong fundamental knowledge of cancer genetics and epigenetics- Experience with next generation sequencing (WGS, RNAseq, ChIP-seq), gene editing (CRISPR), and/or mouse cancer models (transgenic or xenograft models) including prior cancer biology research experience - A PhD or MD/PhD - A Publication record, including first author peer-reviewed publications - Abilty to think creatively and independently and bring a highly motivated, enthusiastic attitude towards scienceIn this role, you will: - Manage and develop a variety of translational projects related to our recently developed Pediatric Translational Medicine Program which utilizes genomic information from a patient’s tumor to guide future therapies- Be expected to contribute and continue to expand upon ongoing projects aimed to validate novel therapeutic candidates identified through loss of function screenings and integrative system biology approacheInterested candidates should include a synopsis of previous research experience (1 page), a personal statement of scientific interests and goals (1 page), a detailed CV, and contact information of three references with your application. 
Requisition ID
2020-39979
Category
Research - Laboratory
Job Locations USA-NY-New York
Posted Date 6 months ago(1/12/2020 4:32 PM)
For more than 20 years, Immigrant Health and Cancer Disparities (IHCD) has worked to identify and eliminate disparities in health and cancer treatment among immigrants and minorities. Housed at Memorial Sloan Kettering Cancer Center since 2011, the IHCD Service offers a wide range of programs for patients, healthcare professionals, and patient advocates. Our team uses a multidisciplinary approach to address gaps in healthcare at the local, national, and global levels. Our community-based programs provide a gateway to health education and services for immigrants and other medically underserved minorities in New York City and beyond. Hours: Initial training M-F 9 am – 5 pm.  The position requires fluency in Spanish-written and spoken. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Coordinator assists with the maintenance of Patient Management and Data Management on clinical studies.  In this role, you will work closely with MSK and each participating institution on data collection, entry and analysis and ensuring data quality and integrity throughout the life of the study. You Have:- Language Requirement - Spanish Fluency- A Bachelor’s degree  - OR -  High school diploma with 2 years medical or research experience- A genuine interest in working in health disparities research- Excellent Communication, attention to detail, information and time management, administrative and Computer SkillsYou Are:- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward- Consistently achieving results, even under tough circumstances- Able to hold yourself and others accountable in order to achieve goals and live up to commitments- 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 obstacles- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances- Interested in medical terminology and science- You are comfortable with or interested in working with and organizing large amounts of dataYou Will:- Be responsible for data collection including utilizing appropriate methodologies to collect human subject information for a research project, database and/or protocol (clinical trial) by reviewing patient charts, existing databases, and other sources within a specified timeframe- Interact with team members and individuals across MSK regarding data input- Generate data reports and deliver to all necessary parties on the progress of research project, database or protocol- Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the research project, database or protocol, and that research protocols are approved by Institutional Review Board and all regulatory documentation is completed- Provide clerical and administrative support, such as filing and scheduling meetings and appointments as needed 
Requisition ID
2019-38719
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 6 months ago(1/8/2020 1:34 PM)
 Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education.https://youtu.be/9R7QoNfmm0w We have an exciting opportunity in our Infectious Disease service as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA) coordinates and maintains the assigned research portfolio for a Service and/or Department.You Will:- Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols. - Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight. - Effectively communicate the overall study progress to various internal and/or external stakeholders, and identify study trends and create/implement solutions. - Perform diverse research-related functions using sound judgment and exceptional organizational skills.You are:- Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders.- Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals.- Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs.You have:- HS Diploma/GED with 2-4 years relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelor’s Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory.- Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required.- Proficiency with the Electronic Medical Record (EMR) system.- Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics.- Knowledge of clinical research data collection processes in accordance with GCP.
Requisition ID
2020-39040
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 8 months ago(11/21/2019 7:36 PM)
The Advanced Light Microscopy Operation of the Molecular Cytology Core Facility at MSK is seeking a Senior Research Scientist/Senior Microscopy Specialist to join their team.  The Molecular Cytology Core Facility is offering a full-time position for a highly motivated person who is interested to apply and further develop his skills to support scientists and students with image acquisition and data analysis. The MCCF is supporting  complex microscopy setups, including Zeiss confocal/Airyscan, Leica confocal microscopes (SP5 on an upright stand,  SP5 on an inverted stand and  SP8/WLL&APDs), widefield bright field/fluorescence microscopes, laser capture microdissection microscope, digital slide scanners and image analysis workstations with a range of software packages, e.g. Imaris, AutoQuant, MatLab, FIJI/ImageJ, Voloom, CaseViewer. We have more than hundred users with a diverse range of applications and imaging needs. The new team member is expected to work with image processing and image analysis in the dynamic environment of basic and clinical researchers, as well as oversee the training of the scientists, using the equipment. As the Senior Research Scientist/Microscopy Specialist You Will: - maintenance of the daily operation of the high-end light microscopes and equipment infrastructure, including instrument performance tests, troubleshooting, alignments- teaching microscopy classes- writing reports, preparing presentations, collaborating in scientific papers- user consultation, training and assistance with routine and advanced light microscopy techniques to ensure correct set up and optimum microscope operation- provide project-based advice for preparation of biological samples, including fixation, tissue sectioning, tissue clearing and expansion microscopy, image acquisition, data processing and image analysis- maintenance and upgrades of the Core infrastructure (network, computers, servers, software) in coordination with the IT team  You Need: - PhD in (Biology, BioPhysics or related fields with several years of work experience with microscopy image processing and image analysisS- Strong service and team-orientation, and excellent organizational, problem-solving and communication skills- Practical experience with data processing, data management, image analysis, programming and advanced imaging techniques- A passion for learning and problem solving- Strong organizational skills, flexibility in working hours and ability to multi-taskInterested candidates should complete the online application and include a CV, cover letter that includes a list of relevant experience and the names of three references.
Requisition ID
2019-38233
Category
Research - Clinical
Job Locations USA-NY-New York
Posted Date 9 months ago(9/25/2019 1:53 PM)
Do you want to be a part of something bigger than yourself? At Memorial Sloan Kettering Cancer Center, we’re running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We are looking for Clinical Research Coordinators (CRC) to join as an integral member of a research team. In this role, and in compliance with all regulatory, institutional, and departmental requirements, you will have ownership of maintenance of data management on clinical studies. If you're looking to expand your horizons and explore your interests in healthcare and medicine, submit your application today.You Are:- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward- Able to hold yourself and others accountable in order to achieve goals and live up to commitments- 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 obstacles- Passionate about medical terminology and science- You are familiar with and excited about working with and organizing large amounts of dataYou Will:- Collect, abstract, and enter data for research projects, databases and/or protocols (clinical trial) including reviewing patient charts, existing databases, and other sources within a specified timeframe- Ensure data quality and integrity throughout the life of the study.- Collaborate with team members and individuals across MSK regarding data input- Generate data reports and deliver to all necessary parties on the progress of research project, database or protocol- Ensure that we are following all appropriate Institutional, State, and Federal regulations throughout the study, and complete all regulatory documentation to ensure that research protocols are approved by Institutional Review Board- Provide clerical and administrative support, such as filing and scheduling meetings and appointments as neededYou Have:- A Bachelor’s degree OR a high school diploma and 2 years of research experience- The ability to commit to at least 2 years- Effective communication, excellent attention to detail, strong information and time management, and administrative / computer Skills- Flexibility in your approach and demeanor to align with the shifting demands of evolving circumstances
Requisition ID
2019-34442
Category
Research - Clinical

Stay in touch!

Register now to join Memorial Sloan Kettering’s Talent Community to receive inside information on our organization and new job opportunities.