Clinical Research Data Specialist

Description - External

The Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinical trials and works in conjunction with a Clinical Research Nurse/Coordinator (CRN/CRC) to ensure accurate and timely delivery of data compilation and submission. Responsibilities include: extracting data from source documents to complete case report forms for oncology clinical trials, responding to data queries, gathering and organizing clinical data, participating in departmental and study related meetings, conducting study initiation meetings and participating in study monitoring visits onsite.

In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families, in a manner that supports the conduct of clinical trials.

Flexibility in work schedule when possible must be maintained to ensure coverage of study responsibilities

Education
Bachelors Degree (Required)
Combination of relevant education and experience may be considered in lieu of degree.

Experience
General Experience in the medical or scientific field (Preferred)
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