**Please upload your cover letter and resume as one PDF** The Development Department’s Digital Strategy & Marketing team is seeking a passionate, strategic, creative, highly motivated Coordinator to join its team. The Digital Strategy & Marketing team manages a revenue-driving, multi-channel digital program. Donations go to pioneering research and patient care at MSK and are vital to creating new and better treatments for cancer patients worldwide. You will:- Collaborate on the development of fundraising and engagement campaigns with an emphasis on digital channels (email, website, paid search, display, and social) that build, maintain, and evolve a first-in-class and integrated donor experience and generate revenue for cancer research and patient care- Help lead the execution of fundraising initiatives from start to finish, driving collaboration with various stakeholders while leveraging and improving internal processes and improving return on investment- Work with team to evaluate the impact of marketing programs in achieving revenue and engagement objectives and create marketing analytics reports as needed- Support team with partner and vendor relationship management- Undertake a diverse and high-volume of daily administrative tasks to ensure the functionality and coordination of the department’s activitiesYou Are:- Mission-driven and passionate about fundraising and proactive in sharing ideas - Detail oriented, organized, and capable of multitasking with enthusiasm and efficiency in a fast-paced environment- A strategic thinker who stays on top of tactical execution, deadlines, and revenue goals- Deeply curious about digital marketing trends, platform capabilities, and best practices- A positive, collaborative team player who takes pride in personal and team successYou Have:- A Bachelor's degree and minimum 3 years in marketing with an intimate understanding of traditional and emerging channels (at least 7 years of relevant experience required in lieu of a Bachelor's degree)- Superior project management skills, with the determination and ability to drive a project from concept to launch- Fundraising and development experience with strong desire to raise funds for cancer research- A keen interest and developing skillset in marketing analytics- The ability to think creatively - Strong interpersonal and written communication skills- A detailed eye and interest in perfecting copy, ensuring high quality, and maintaining brand integrity- Experience with Adobe Creative Suite#LI-POST
**A cover letter is required to be considered for this position. Please indicate which position you are interested in your cover letter (NYC, or markets outside of NYC). Please upload your cover letter and resume as one PDF or WORD document** Cycle for Survival is seeking a passionate, highly motivated, and action-oriented Development Officer to join its national Recruitment and Fundraising team.Working directly with the Recruitment and Fundraising team, you will be responsible for the strategic recruitment and stewardship of Cycle for Survival’s participants and donors. You will assist in carrying out fundraising initiatives and provide highly personalized assistance to all participants and donors. In addition, you will support the Regional Manager in the development and strategic growth of your respective markets. You will:- Provide a highly-personalized level of customer service to the devoted and growing Cycle for Survival community.- Bolster and maintain a vast pipeline of individual and corporate donors and participants by email, phone and in-person.- Proactively cultivate and solicit participants, donors and prospects to deepen relationships and increase giving.- Implement a strategic communications plan and timeline to meet and surpass the ambitious recruitment and fundraising goals of the program.- Regularly solicit, coordinate and lead pitch presentations to all levels of corporate leadership at a variety of companies.- Actively collaborate with the Fundraising Events team on all activities and initiatives associated with the recruitment and fundraising efforts of the respective markets.You are:- You enjoy working with people and building strong relationships.- You are detail-oriented and capable of handling multiple high-volume projects and relationships simultaneously.- You are a team player who takes significant pride in your individual success, as well as the success of the team.- You aren’t afraid to set goals and create strategies to achieve them.- You have exceptional verbal and written communication skills.You need:- A Bachelor’s Degree is required- Proven success in building strong interpersonal relationships- Excellent written and verbal communications skills- At least 5-7 years of relevant experience. A background in fundraising, finance, communications, sales or account management would be beneficial.Please note: - This recruitment and fundraising position is based in NYC. - This position will require evening and weekend work as well as occasional travel based on market.- Candidates seeking an event planning position should consider other opportunities.CYCLE FOR SURVIVAL:Cycle for Survival is the national movement to beat rare cancers where 100 percent of every donation funds rare cancer research. About half of all cancer patients are fighting a rare cancer, and they often face limited or no treatment options. Since 2007, Cycle for Survival has raised more than $220 million through its signature indoor team cycling events across the U.S. to help fund pioneering rare cancer research led by Memorial Sloan Kettering Cancer Center, which owns and operates Cycle for Survival. Together with the movement's founding partner, Equinox, Cycle for Survival has supported innovative clinical trials, research studies, and major research initiatives.#LI-POST
The Department of Epidemiology and Biostatistics, a group made up of 35 doctoral and MS level biostatisticians, is seeking a highly motivated and successful individual to join them at the doctoral level in the newly created track of Principal Biostatistician. The primary responsibilities of this position are to:• Participate in collaborative research between the Biostatistics Service and one or more of clinical, translational and basic science groups in the institution;• Depending on the nature of the collaboration, take full responsibility for all aspects of the collaboration, or participate along with a faculty biostatistician;• In the context of a collaboration study, supervise the work of a research biostatistician or a data analyst. The ideal candidate should have: • A doctoral degree in statistics, biostatistics, or a related field• Proficiency in a statistical programming language (such as SAS, Stata, and R)• Experience of collaborative research (including creating and maintaining data files, writing application programs within a statistical software, analyzing data, interpreting the results, and contributing to manuscript writing).• Excellent verbal and written communication skills• A strong commitment to statistical collaborations with medical and basic science investigatorsPlease note that when submitting the online application applicants are required to submit their CV, in addition to a cover letter outlining the reasons for their interest in the position including names/contact information of 3 references.#LI-POST
The Precision Pathology Biobanking Center (PPBC) is a newly established research center at Memorial Sloan Kettering Cancer Center. A central pillar of the Center is the collection, database annotation, and banking of human biospecimens. Our team of biobanking professionals procures surgical and biopsy research samples from over 8,000 patients per year. Our samples are a key prerequisite for high-impact cutting-edge basic, translational, and clinical trial research at MSK. We are looking to recruit highly motivated Research Technician/Assistant to join our active high-volume tissue and body fluid biobanking team. You Will: - Processes human surgical specimens in timely fashion and following specific SOP and individual protocol requirements- Ideal for highly motivated individuals with opportunity for academic development, individual research projects, and growing responsibilities- Highly collaborative environment with physicians, scientists, technologists, and comutational/database specialists- Extracts relevant clinical information and enters data in biospecimen databases- Works with surgical pathology prosecting teams to procure tissue- Helps develop novel protocols for rapid, high-quality specimen procurement- Independently designs, plans, and sets up new protocols for biospecimen collection and processing - Participates in Center Quality Assurance and Quality Improvement activities- Works with the Center’s IT team to improve and implement biobanking software solutions- Uses database tools to query and retrieve inventory- Works well in a large team and communicates wellYou Need:- Bachelor or Masters in relevant scientific field (biochemistry, molecular biology, premed, pharmacology, anatomy/physiology, or related fields) with at least 5 years of work experience in a biological laboratory environment required- Medical graduates are strongly encouraged to apply. - Knowledge of anatomy/physiology and experience with medical records is a plus.- Comfortable with computer use (especially databases); some coding/programming experience/interest and interest in biostatistics/bioinformatics ideal- Formal licensing as a clinical technician is not required Hours: M-F, 9am-5pm
The Manager, Biomedical Systems manages new and evolving technologies and their integrations supporting the medical equipment devices and overall medical equipment management program. This position is responsible but not limited to the testing and evaluation of technologies and technical issues such as cybersecurity, RFID / RTLS, as well as the integration and development of clinical applications, such as the institutional asset archive and database. This position is responsible to support all regulatory and operational functions, such as inventory management including planning, receiving, deployment, and documentation. Equipment may include clinical, radiological therapy, high energy devices, surgical system devices and supporting integrations. Supervises the work of engineers, technicians, external third party resources and orients and trains employees in job duties and use of equipment. This role will participate in the development and implementation of departmental and institutional biomedical technology goals and objectives, and interface with other biomedical engineering teams, physicians, scientists, medical and administrative staff in clinical and research programs and projects. You Will:- Inspects, repairs, calibrates, and maintains biomedical equipment systems.- Performs preventive and corrective maintenance on a wide variety of biomedical equipment.- Plans, tests, evaluates and installs new equipment systems.- Coordinates, directs, and supervises the work activities of biomedical technicians and staff engineering specialists.- Communicates knowledge of biomedical equipment technologies to staff and coworkers to improve equipment operation and services.- Implements suggestions for modification and changes to equipment or systems in conjunction with manufacturer’s input and needs of medical staff to enhance the performance, reliability, functionality and safety. - Documents and records information on equipment service/repair in a computer database; generates reports as requested by supervisor.- Performs medical device cybersecurity assessments and maintains documentation for equipment/systems. You Have: - Masters degree in Biomedical engineering or related field- 7-10 years of relevant experience - Knowledge of QC testing and maintenance of imaging and robotic equipment.- Experience in the following areas: surgical engineering, computers/electronics design, information management, teleconferencing, streaming digital video, image archiving, voice recognition robotic, MPEG video compression, biomedical/surgical facility design and planning#LI-POST
We are:At Memorial Sloan Kettering, we take a team approach to caring for children, adolescents, and young adults with cancer. Our experts share the goal of curing child and returning him or her to a life focused on family, friends, and the future. We care for young people with all types of cancer, from the most common to the rarest, and at any stage, including a cancer recurrence. You are:- Capable of building strong customer relationships and delivering customer-centric solutions.- 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 will:- Provide Child Life services to pediatric patients based on an understanding of child development and the impact that illness, injury, disability and hospitalization have on this process.- Develop and execute group activity programs- Plan interventions specific to the impact of the health care- Provide guidance for the family in understanding and dealing with hospital regulations and procedures, while facilitating opportunities for parents for actively continue their parenting role.- Maintain records, statistics, activity calendars, schedules, and other appropriate documentationYou have:- Bachelor’s degree in Child Life, Recreation Therapy, Art Therapy, or Special Education; Master’s preferred- 1-2 years of related experience- Child Life Specialist Certification OR completed requirements with plans to take exam within one year of hire Hours will vary between 8:00am-7:00pm and include a weekend rotation, as well as some holidays #LI-POST
We are seeking Radiologic Technologists to join our Radiology team at our main hospital in Manhattan. See below for shift information. You are: • Committed to high standards of productivity.• Motivated to provide exceptional customer service.• Willing to take action and eager to tackle new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.• Adaptable in your approach and demeanor in real time to match the shifting demands of different situations.• A good decision maker, with shown success of making timely decisions that keep the organization moving forward.• Adept at planning and prioritizing work to meet dedications aligned with organizational goals. You will:• Under the direction of the Diagnostic Radiology Manager, performs routine radiographic procedures on patients of all age groups at the technical level which does not require supervision.• Coordinate departmental patient flow activities as needed. You need:• A High School degree, plus 2 years Accredited Radiological Technology Education.• At least 3 years of relevant experience.• NYS General Radiography license and ARRT certification. #LI-POST
We are seeking a Clinical Research Supervisor (CRS) to join our dynamic team Thoracic Oncology Service in the Department of Medicine. As a CRS, you will supervise the day-to-day activities of 6-10 Clinical Research Coordinators (CRCs) to ensure efficient and effective operations. You will be responsible for data management activities and for data integrity associated with clinical research. Also, you will have the opportunity to participate in special projects and task forces as determined by management. You will manage several research protocols, including investigator initiative trials, industry-sponsored studies, as well as bio-specimen protocols. The Thoracic Oncology Service, led by Service Chief Dr. Charles Rudin, MD PhD & Research Director Dr. Gregory Ridely, MD PhD, is changing how thoracic cancer is treated. Drawing on the careful genetic analysis of lung cancers, we have subdivided this group of diseases into smaller subsets, each sensitive to highly specific anticancer treatments that can often be given in pill form. These treatments are spurring remarkable changes among patients with advanced lung cancers who would otherwise receive classic chemotherapy. You will:- Staff Management and Development - Participate in the orientation, training and supervision of CRCs; participate in facilitating departmental trainings; align staff and resources with appropriate protocols and research needs; and maintain workflow consistency among staff with standardized processes.- Operation Management - Ensure that workflow is managed and monitored to meet departmental and service needs; assist the Clinical Research Manager (CRM) with protocol activation, especially with start-up activities; monitor research portfolio for workload by appropriately managing and identifying service needs.- Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that the research project is carried out as planned.- Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Also, you will ensure that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written.- Data collection - Utilize appropriate methodologies to collect patient/human subject information for research projects, databases, and/or protocols.- Data reporting - Generate reports to all necessary parties (institutional and federal) on the progress. You will prepare data for analysis, monitoring visits and audits.- Clinical Research Billing Management - Implement Principal Investigator's decisions regarding Patient-Care Costs (both billable and non-billable), and ensures that research non-billable services are not billed to patients/human subjects or insurers. Also, you will assist manager with billing reconciliation.- Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. You will provide leadership, organizational, creative, or clerical support to established and new research 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 the organization moving forward.- Eager to foster talent and support people in meeting their career goals and the organization's goals.You Have:- A bachelor's degree with at least 3 years of clinical research experience OR a high school diploma with 6 years of clinical research experience- Supervisory experience and experience with high volume trials is strongly preferred.- 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) is critical.- Strong time management/project management skills.- Knowledge of oncology-specific terminology is helpful.- Experience in the use of various electronic data management systems. Strong Data management skills, including database design preferred.- Basic knowledge of Microsoft suite (PowerPoint, Word, Access, Excel) and Teamshare.
Clinical Nurse – Benign Hematology/Anti-Coagulation Office PracticeHours: Full time Four days X 10 hour days flexed Monday - Friday We are:- Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment- http://careers.mskcc.org/nursing/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 maintain high standards of nursing care within the organization.- Actively seeking new ways to grow and be challenged, using both formal and informal development channels.- 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:- Work within a Nurse-Physician based Ambulatory Care Practice Model.- Provide care for a caseload of patients receiving treatment for benign hematological disorders and patients requiring anti-coagulation management in the outpatient setting.- Learn to manage hematological malignancies, thrombotic diseases and also hemorrhagic disorders- Perform patient assessment, provide symptom management and patient and family education.- Act as part of a multidisciplinary team to provide continuity of care throughout various stages of treatment and follow-up.- Participate in the implementation of clinical support programs to ensure optimal care throughout the healthcare continuum. You need:- New York State RN license and BSN- 1.5 years of related medical/surgical experience required- Hematology experience strongly preferred- Ambulatory care experience preferred
MSK is at the forefront of a digital and data transformation that will revolutionize the way the world understands and treats cancer. We are looking for an accomplished enterprise data architect with a deep understanding of modern data architecture concepts and technologies to help lead this journey. The Enterprise Data Group at MSK has developed and maintains one of the most robust oncology data ecosystems in all of healthcare. The integration of clinical, genomic, operational, and financial datasets has led to countless insights, but we are just beginning to capture the full value of our unstructured notes and images by way of AI and machine learning. If you are passionate about data and building innovative, collaborative solutions that will help transform the rapidly-evolving field of oncology, we have an opportunity for you! You will:- Build a future state of the art architecture that will empower day-to-day operations, and the MSK research and scientific community- Provide data management vision by building data models, diagrams, architecture topologies, roadmaps, and plans for implementation and rollout of new technologies into existing and future architectures- Develop robust, scalable, resilient, and secure data architecture solutions that enrich and protect institutional data assets- Work closely with the Data Governance Office to ensure that a proposed data architecture solution fully supports data governance-related requirements and are coordinated the platforms- Collaborate with senior IT and hospital leadership to gather enterprise data requirements in order to implement and communicate complex technical solutions across varying disciplines- Be a strong communicator, open to new ideas and implementing technologies, and flexible in high pressured environments- Feel comfortable working with large teams including high level executives and be a contributor in a collaborative organization You will:- End-to-end data management and architecture experience including complexities of a large enterprise data architecture framework- Solid grasp of modern technologies and integration architecture disciplines such as hybrid cloud, API’s, streaming technologies, event-driven systems, self-service data platforms and analytics/Machine Learning/Artificial Intelligence- Experience in cloud based data management solutions: AWS/Redshift, Google/BigQuery, MS Azure, Snowflake, IBM Cloud Pak- Demonstrated the ability to understand and distill knowledge of emerging technologies, as well as conduct proof-of-concepts of well-established and innovative enterprise software tools- Experience with design, conceptual, logical, physical, strong knowledge of relational databases, SQL, and columnar databases- Good interpersonal skills, written and verbal communication skills, and a strong proficiency in the prioritization and implementation of objectives and key results #LI-POST
The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Research Project Manager (RPM). As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Research Project Manager is responsible for providing support to the Clinical Operations Program Manager and Chief Executive Officer for multi-center clinical trial activities. Commitment to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role. 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. You will: - As determined by manager, manage staff and their development - Participate in the orientation, training and supervision of Research Project Associates. Participate in facilitating departmental trainings. Align staff and resources with appropriate protocols and research needs. Maintain workflow consistency amongst staff with standardized processes. - Manage and champion a highly complex multi-institutional, international, prospectively designed clinical registry, in addition to clinical trials as required by the Company.- Design and oversee operational and quality plans including concept development, correlative and translational design, protocol and informed consent drafting, safety and regulatory document drafting, monitoring and quality plan drafting, etc.- Communicate effectively by establishing strong working relationships with a diverse matrix of clinical trial sites, investigators, pharmaceutical & biotechnology executives, registry executive committee members, and other important stakeholders.- Synthesize complex clinical, regulatory, and other 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 (includes Project Management Plans, Safety Management Plans, Monitoring Plans, Meeting Minutes, etc.).- Communicate and work effectively with all stakeholders of the PCCTC – Executive Leadership, Clinical Operations, Informatics, Business Management, Budgets & Contracts, Editorial, etc.You need:- 4-7 years of relevant (clinical research) experience, or as determined by hiring manager.- A Masters degree is preferred.- Proven 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 and/or large scale registry projects is a plus. #LI-POST
At Memorial Sloan Kettering, our social workers play a meaningful role in providing emotional support and guidance to people with cancer, as well as friends, families, and caregivers. We are seeking to hire a Clinical Social Worker II to provide comprehensive bio-psychosocial assessment and follow-up to adult patients and families in response to social, psychological and environmental needs related to the impact of diagnosis, admission, treatment, discharge, continued care and post-treatment. This position will be located in both the Ralph Lauren Center for Cancer Care and the Brooklyn Infusion Center. In this role, you will report to a Supervisor within the Department of Social Work. If you'd like to learn more about our Social Work department, click here for more information. You Will:- Conduct screening and bio-psychosocial assessment of patients and families to assess their distress & develop ongoing clinical plan.- Provide clinical interventions and modification of psychosocial plan, ongoing clinical assessments, advocacy, resources and practical advice for patients and their families.- Collaborate with interprofessional team to address ongoing patient needs.- Assist patients/families in accessing appropriate psychosocial services along the continuum of care.- Identify the unique needs of assigned service; develop and implement appropriate interventions and programs.- Produce quality documentation in the medical record and all written correspondence; and prepare Philanthropic Budget Sheets and other departmental-related documentation.- Focus on professional development through supervision of student interns; participating in team consultation, teaching and research, presentations at national conferences and contributions to the social work/oncology literature.- Participate and serve on department-wide committees. Work with Supervisor, Practice Group Leader and/or Director of Social Work on special projects as assigned.You Need:- A Masters degree in Social Work and NY-LCSW are both required.- At least 1 year of post master’s work experience in a hospital.- Strong clinical skills with individuals, families and groups.- Proficiency in Spanish is required.- Experience in oncology and/or palliative care in a hospital setting preferrred- Excellent written and oral communication skills.- Proficiency in Microsoft Office applications.#LI-Post
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.
We have an exciting opportunity in our Radiation Oncology 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.
Incredible Clinical Nurse Opportunities for experienced Operating Room Nurses! We are:The Josie Robertson Surgery Center (JRSC) is a first-of-its-kind, freestanding outpatient and short-stay cancer surgery facility that delivers exceptional care to patients while utilizing the latest in surgical technology. The Center re-designs the way in which perioperative cancer care is provided, with an emphasis on innovation, continuous data-driven improvement, and an optimized patient experience. The opening of this new facility marked a new direction at MSK by focusing expertise on the delivery of high quality, cost effective surgical treatment of cancer that will complement a long established reputation for excellent surgical care of patients with advanced, complex cancers. Through the JRSC, MSK has developed a safe, efficient, patient-friendly, high-volume, high-quality, extended ambulatory surgical program committed to continual quality improvement and patient and provider satisfaction.You are:- An experienced Operating Room (OR) Registered Nurse (RN)- A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization- Actively seeking new ways to grow and be challenged- Approachable – someone who is comfortable with diverse groups of people and able to make others comfortable with you- An effective communicator- Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasmYou will:- Provide primary nursing care in the Josie Robertson Surgery Center Operating Room- Will provide coverage at the Main Campus Operating Room as needed- Perform duties under the direction of the nurse leaderYou need:- NYS RN license- BSN- BLS- Minimum of 1.5 years of operating room RN experience required- CNOR certification highly preferred Shift:- 10 hr variable shifts between 7am and 11:30pm, Monday - Friday, with weekend rotation as needed.
Prostate Cancer Clinical Trials Consortium (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. Incubated within Memorial Sloan Kettering (MSK) and in 2014 established as an independent entity – the PCCTC, LLC – it 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. PCCTC is hiring for a Senior Clinical Data Manager. In this role, you will provide requirements specifications for instrument design (eCRFs/databases, edit checks) for data acquisition for clinical trials performs data cleaning activities to review, analyze and validate data to ensure completeness, integrity and accuracy. Works on complex assignments and projects where analysis of situations requires an in-depth evaluation of variable factors. Provides 2nd level project management support and mentoring of fellow Clinical Data Managers and departmental users. Manage projects involving multiple teams. Exercises judgment in selection methods, techniques and evaluation criteria for obtaining results. Networks with key contacts outside own area of expertise. You will:- Design Case Report Forms(CRFs)/database requirements/specifications (includes field definitions, automatic edit checks, indication of critical variables and CRF Completion Guidelines).- Assist in design of queries using SQL to check for missing or inconsistent eCRF data.- Understand, update and optimize existing queries/reports.- Query tracking and resolution (i.e. correspondence with investigator sites to obtain resolution to queries).- Analyze data to find potential issues/inconsistencies/areas, etc.- eCRF data validation (i.e. scrubbing , cleaning, query generation, applying data handling conventions).- Train users on EDC functionality.- Provide necessary documentation in compliance with existing standard operating procedures, regulatory guidelines, etc.- Maintain necessary clinical trial conduct documentation (includes Data Management Plans: database specifications, electronic edit checks, External Data Transfer Plan, etc.).You Are:- Comfortable working in a fast-paced environment.- 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.You Have:- 5 years or more of clinical data management and clinical research experience or as determined by hiring manager.- A Bachelor's degree is preferred, or 4 years of job-related work experience can be accepted.- Certified Clinical Data Manager Certification (CCDM) preferred.- 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).- Excellent computer skills including proficiency MS Office products.- Experience with SQL/SAS/Business Objects, any reporting tools and programing languages preferred.- Experience working in an FDA regulated environment a plus.- Experience and/or desire to learn working with various EDC systems: Medidata Rave, Caisis, InForm, etc.#LI-POST
Are you interested in playing a key role in integrating optimal protocol activation functioning for clinical research? 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. Our Protocol Activation Core was created in January 2018. We are a centralized team handling protocol activation for all clinical trials at MSK. We are seeking a Protocol Activation Manager to join our dynamic team. In this role, you will lead the activation of assigned clinical research studies and coordinate all aspects of protocol activation. You Will:- Direct and lead all protocol activation for assigned protocols ensuring customer focus, activation goals and accountability- Manage complexity and obtain clear understanding about protocol hypothesis, scientific background, research rationale, participant work flow, potential side effects, risks and benefits, costs, etc to ensure optimal activation strategy and appropriate reviews.- Collaborate and communicate effectively with all internal and external stakeholders on assigned protocol areas to have a complete and full understanding of the protocol and ensure rapid activation.- Assess complex protocols quickly to plan an effective activation path and manage all submissions to review committees, sponsors, CRA units and clinical departments per institutional guidelines to meet time to activation expectations while ensuring high quality.- Ensure that all protocol documents are clear and follow Federal Regulations and Institutional policies.- Advise, assist, and guide Principal Investigators in appropriate responses to sponsors, review committees, and units.- Ensure Principal Investigators and Clinical Research Managers (and others as needed) are notified of protocol status throughout the entire process through metrics, dashboards, and reporting.- Track protocols as they move through the review process, involving necessary staff and Leadership as required.- Ensure all required reviews, approvals, budgets, contracts, logistic and feasibility reviews, site initiation visits, order sets/CTMS calendars and drug/device are in place (if applicable) and all regulatory and institutional activation steps have occurred. - Determine when a protocol can be opened to patient/participant accrual.- Write informed consent document and convert model consents to MSK template. - Negotiate consent language with external Industrial sponsors, ensuring that sponsor(s) understand expectations of MSKCC’s IRB and utilization of MSK standard text.You Are:- Able to interpret complex research protocols quickly and discern the explicit and implicit items needed for activation.- Able to navigate and champion protocols through a complex system involving various internal and external departments involved in human research studies.- Able to hold yourself and others accountable in order to achieve goals and live up to commitments. - Focused on continuous improvement, knowing the most effective and efficient processes to optimize work flow.- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. You Have:- A Bachelor's degree (preferred), with 4-7 years of clinical research experience- Experience with Human Subjects Protection, GCP and GMP standards, FDA/EMA requirements, Quality Standards and Systems - Experience working with sponsors- Experience with protocol development #LI-POST
We are seeking an experienced Research Project Manager (RPM) for the Pediatric Research Oncology Xenografting Consortium (“PROXC”). PROXC is a network of academic research centers engaging in collaborative research to enable and facilitate basic and translational research that provides clinical and therapeutic insight for pediatric cancers using xenografts as validation tools. You Are:- A strong project manager with the ability to create project plans, lead project teams, and communicate with various stakeholders.- An excellent communicator that will be able to explain, interpret, share and present information on PROXC related projects to investigators, staff, and appropriate external contacts.- Excellent at time management, especially when involved with simultaneous management of multiple projects.You will:- Manage the functions and activities of PROXC.- Manage the development of a robust workflow for tumor tissue collection and cancer model (PDX) generation.- Manage the development of a diverse portfolio of clinically annotated and molecularly characterized cancer models- Be responsible for development of a biobank of models for future investigations. - Engage with external collaborators on project development and execution inclusive of project budgets and contracts.- Have in-depth knowledge of the processes/procedures associated with clinical practice, clinical research, and/or a strong information systems expertise in the latest technologies.You need:- A Bachelor’s degree with at least 4 years of experience in clinical research and/or other applicable research investigation. Relevant graduate work would be considered in lieu of minimum experience.- Master’s degree preferred.- Experience with Microsoft Excel and Access, database knowledge.- Ability to solve problems by using a logical, systematic, sequential approach.- Excellent interpersonal, verbal and written communication skills.- Strong organizational, prioritization, and project management skills.- Proven ability to manage clinical research projects with strict deadlines.- Must have a 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). #LI-POST
We Are:The Department of Pathology at MSK is a dedicated, diverse group known for their expertise, ingenuity, and compassion. Working in a highly motivating environment, the group receives a complex variety of more than 110,000 specimens annually and performs more than 50,000 molecular diagnostic and cytogenetic tests. More than 600 staff members are spread across four laboratory services: surgical pathology, hematopathology, cytology, and molecular diagnostics.Pathology provides laboratory support for the Mohs micrographic and dermatologic surgery program and supports MSK’s research mission through the division of experimental pathology. We’re also advancing the field of digital pathology through our slide scanning and computational pathology efforts. All of our laboratories are equipped with state-of-the-art equipment, such as ThermoFisher senior grossing stations with advanced camera optics and touch screens, laser capture microdissection capabilities, telecytology remote microscopy, advanced flow cytometry panels, and Illumina sequencing instruments. The Department of Pathology is currently seeking a Histology Technician. You Will:- Process tissue from all patients for routine histopathology preparations.- Performs special procedures.- Process fresh and fixed tissue specimens for surgical, autopsy, and investigative histopathology preparations with minimal supervision.- Performs assigned quality control procedures. You Have:- Associate’s Degree in Biology or chemistry required OR NYS Clinical Laboratory license- 2-4 years of experience in histopathology required- NYS Clinical Lab Technologist/Clinical Lab Technician/Certified Histology Technician required Hours: M-F, 9am-5pm
We are providers:- Compassionate, evidence-based nursing to Oncology patients and their families living with cancer in a healing and creative environment- Dedicated to relationship based care for patients and staff- Involved in extensive clinical trials growing cancer treatment.- Enrolled in ongoing educational opportunities and skill development- Nursing at MSKYou are:- Willing to act and eager to adopt new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- A creative decision-maker, with shown success at making timely decisions that maintains excellent standards of nursing care within the organization.- Actively seeking new ways to grow and be challenged, using both formal and informal development channels.- Approachable and skilled with providing care to diverse groups of people.- An effective communicator, capable of resolving how best to reach different audiences and executing communications based on that understanding.- Flexible in your approach and demeanor to align with the shifting demands of evolving circumstances- Capable of building strong customer relationships and delivering customer-centric solutions.You will:- Work within an Ambulatory Care Practice Model.- Manage a select caseload of patients receiving chemotherapy/biotherapy on an outpatient basis- Administer chemotherapy/biotherapy, perform patient assessment, and provide symptom management and patient and family education.- Participate in the implementation of patient education and clinical support programs to ensure optimal care throughout the healthcare continuum- Participate in an individualized training/orientation program geared to providing nursing care in ambulatory setting.- Act as part of a multidisciplinary team to provide continuity of care throughout various stages of Oncology treatment and follow-up.You need:- New York State RN license and BSN- 1.5 years of related chemotherapy experience required- Chemotherapy certification strongly preferred.- Medical Oncology or Breast Oncology experience strongly preferred- BCLSHours: Part time two days x 10 hour days flexed Monday - Friday #LI-MM1