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Senior Study Coordinator
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$54,000 - $63,000 a year
Full-time
- The Senior Study Coordinator (SC) works on clinical and translational studies derived from the Integrated Imaging Program for Cancer Research (IIPCR).
- By performing these duties, the SC works with the PI, IIPCR program, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical/translational study.
- Work with PI to develop and submit the study protocol and protocol amendments for the IRB and other regulatory documents (e.g., Protocol and Review Monitoring Committee, Data and Safety Monitoring Board) as needed, including the development of new measures.
- Design and/or enhance databases, data forms and tools (e.g., patient/human subject calendars, schedules, tracking logs) to facilitate patient consent and specimen collection as needed for assigned research projects,
- Collaborate with members of the research and care teams across Montefiore-Einstein Cancer Center regarding data input.
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