Responsibilities

The Clinical Scientist will contribute to the development of clinical trial protocols, monitor clinical trial data at study sites ensuring adherence to protocols and GCP guidelines, perform data review and reconciliation, review clinical data to assess safety and efficacy, support the development of clinical documents, maintain knowledge of the therapeutic area and disease state, assess clinical data for safety concerns, conduct literature reviews, and collaborate closely with cross-functional teams including clinical operations, regulatory affairs, medical affairs, biometrics, and project management to ensure data integrity during the clinical development process.