Clinical Data Specialist
5 dni temu
Your Role
As a Director, Medical Review Scientist, you will be responsible for performing medical review activities across multiple oncology studies with a wide range of therapeutic modalities and tumor types.
Key Responsibilities
- Develops a Medical Review Plan (MRP) for the study, which details the scope of the medical review and appropriate timelines s/he performs on the study data.
- Collaborates with the Data Management and Clinical Development team to identify program, trial or data risks, creates, and implements mitigation strategies.
- Supports the Data Management team in ensuring the eCRFs and eCRF completion guidelines accurately reflect the patient population under study and the scope of the protocol.
- Requires a close collaboration with the study's Clinical Development team (i.e., Study Physician, Clinical Scientist) as well as Patient Safety to discuss/review complex medical questions and concepts.
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