Senior Clinical Research Data Specialist
About The Position
The Senior Clinical Research Data Specialist supports data collection, analysis, and reporting for the Office of Clinical Research (OCR) on assigned Phase I, II, or III oncology clinical trials. Working with a Clinical Research Nurse/Coordinator (CRN/CRC), the specialist helps ensure accurate and timely compilation and submission of trial data. The role also interacts with institutional investigators, healthcare team members, service line members, and research participants and families in support of clinical trials. Flexibility in work schedule must be maintained when possible to ensure coverage of study responsibilities.
Requirements
- Bachelor's degree required, or a combination of relevant education and experience may be considered in lieu of a degree.
- Five years of experience in a related clinical research role required.
Nice To Haves
- Two years of experience with Clinical Research Data Management.
Responsibilities
- Extract data from source documents and complete case report forms for oncology clinical trials.
- Respond to data queries.
- Gather and organize clinical data.
- Participate in departmental and study-related meetings.
- Conduct study initiation meetings.
- Participate in onsite study monitoring visits.
- Work with a Clinical Research Nurse/Coordinator to support accurate and timely data compilation and submission.
- Interact with investigators, healthcare team members, service line members, and research participants and families in support of clinical trials.
- Maintain flexibility in work schedule when possible to ensure coverage of study responsibilities.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
