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A clinical-stage biotech company is seeking a Clinical Scientist to support the development of innovative small molecule therapies targeting chronic diseases such as cardiovascular, metabolic, and pulmonary conditions. Using advanced structure-based drug discovery technology, this organization is led by a globally experienced team of drug developers.
Location: Onsite, South San Francisco (4 days/week required)
Key Responsibilities
Contribute to clinical development plans, study protocols, and regulatory documents (IND, IB, NDA, etc.)
Participate in medical monitoring activities including clinical data review and generation of insights
Support investigator meetings, protocol trainings, and regulatory communications
Review literature and support scientific publications and presentations
Collaborate across functions (Data Management, Biostats, Safety) to ensure high-quality, compliant study execution
Analyze clinical trial data, monitor safety trends, and support decision-making in dose escalation and study design
Support case report form (CRF) design, protocol deviation reviews, and query resolution
Advanced degree (PhD, PharmD, or Master's) in life sciences with 3-4+ years of clinical research or drug development experience
Strong knowledge of clinical trial operations, GCP, and regulatory standards
Proficient in data review, study documentation, and software tools (e.g., EDC systems, Microsoft Suite, Spotfire/Tableau)
Excellent communication, project management, and cross-functional collaboration skills
Prior experience in a biotech or fast-paced R&D environment preferred