About this role

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

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

Clinical Scientist – Freelance

Key skills