Manage ongoing departmental projects and build processes to ensure that goals are met.
Assist with high-level department projects requiring data management support; provide data entry solutions as needed.
Provide leadership and/or organizational, creative, or clerical support to established and new research initiatives.
Ensure that all appropriate institutional, state, and federal regulations are followed in conducting a research project, throughout database construction, or in carrying out a research protocol.
Track the progress of investigator-initiated projects throughout the life cycle of the project and assist in the procurement and processing of specimens, as needed.
Use appropriate methods to collect patient/human subject information for a research project, database, and/or protocol.
Extract, compile, and analyze data, and generate reports to all necessary parties on the progress or results from the research project, database, or protocol, as needed.
Communicate with staff at all levels (principal investigators, clinical, and research support staff).
Act as a technical liaison between clinicians, data managers, and clinical research support staff providing expertise to facilitate project delivery.
Assist in problem-solving and issue resolution using appropriate testing and troubleshooting techniques, and serve as an escalation point and subject matter expert to resolve complex issues.
Perform regular audits to ensure that collected data is complete and accurate and that the research project was carried out as outlined.
Participate in or coordinate both interdepartmental and intra-departmental organization-wide research projects as required. Participate in special projects and task forces as determined by management.
At least 3 years of relevant (clinical or genomic research) experience
Must be able to work independently, be flexible, and meet tight deadlines.
Experience in genomic analysis, clinical 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).
Internal Number: 2020-42484
About Memorial Sloan-Kettering Cancer Center
As one of the world's premier cancer centers, Memorial Sloan-Kettering Cancer Center is committed to exceptional patient care, leading-edge research, and superb educational programs. The close collaboration between our physicians and scientists is one of our unique strengths, enabling us to provide patients with the best care available today as we work to discover more effective strategies to prevent, control, and ultimately cure cancer in the future. Our education programs train future physicians and scientists, and the knowledge and experience they gain at Memorial Sloan-Kettering has an impact on cancer treatment and the biomedical research agenda around the world.