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Important Note for MSK Employees:
Responsible for data/project management activities and for data accuracy and integrity associated with clinical research within the disease management team and/or service specific level. Participates in special projects and task forces as determined by management.
You will:
- Utilize appropriate methodologies to collect patient/human subject information for a Research Project, database, and/or protocol.
- Biospecimen collection management
- Management and tracking of liquid biopsy projects
- Participate in special projects and task forces as determined by management.
- Generate reports to all necessary parties on the progress of the Research Project, database, or protocol, as needed.
- Assist in managing departmental data.
- Communicate with staff at all levels (principal investigators, clinical and research support staff).
- Perform regular audits to ensure that the data collected is complete and accurate and to ensure that the Research Project was carried out as outlined.
- Ensure that all appropriate Institutional, State, and Federal 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 creates processes to ensure that goals are met.
- Participate or coordinate on both interdepartmental and intra-departmental organization-wide Research Projects as requested.
- Provide leadership, interpersonal, creative, or clerical support to established and new research initiatives.
- At least 2 years of relevant (human subjects research) experience (1 year with Masters).
- Must be able to work independently, be flexible, and meet tight deadlines.
- Experience in human subjects research and/or other applicable research investigation. Relevant graduate work would be considered in lieu of minimum experience.
- Microsoft applications, database knowledge a plus.
- 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).
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