Clinical Data Specialist (part time)
The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quality expected for reporting to Sponsors and regulatory bodies. Participate with auxiliary teams involved in study set up, conduct, and data cleaning of clinical trials.
This is a part time position that will work approximately 20 hours per week between the hours of 7a-5p.