vom 19.03.2026
The Clinical Scientist is responsible for providing scientific support to clinical development programs, contributing to the planning, execution, and interpretation of clinical studies while ensuring scientific quality and regulatory compliance.
Responsibilities: Contribute to the scientific design and implementation of clinical studies, including protocol development and study documentation. Provide scientific input throughout study start up, conduct, and closeout to ensure data quality and adherence to protocol. Review and interpret clinical data to identify trends, potential risks, and scientific insights. Collaborate with cross functional teams including clinical operations, biostatistics, data management, regulatory, and medical teams. Support preparation of clinical and regulatory documents, reports, and presentations.
Requirements: Advanced scientific degree in life sciences, biomedical sciences, or a related field. Experience working in clinical development or clinical research within the pharmaceutical, biotech, or CRO environment. Solid knowledge of clinical trial methodology and GCP principles. Ability to analyze and interpret complex clinical data. Strong written and verbal communication skills. Ability to work effectively in a collaborative and fast paced environment. Experience in neuroscience or central nervous system indications is required.
This is a part time freelance opportunity with an expected commitment of approximately 8 to 16 hours per week.
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