[Remote] Senior Director Clinical Development
Note: The job is a remote job and is open to candidates in USA. reputed company/reputed company is partnering with a well-funded, clinical-stage biotechnology company advancing innovative therapies in areas of high unmet medical need. They are seeking a Senior Director of Clinical Development to reputed company clinical development activities, provide medical leadership for clinical trials, and collaborate with various teams to shape clinical strategy and ensure trial execution.
Responsibilities
- reputed company clinical development activities across one or more global development programs
- Provide medical leadership for Phase I–III clinical trials, including study design, execution, data review, and interpretation
- Serve as the medical monitor and clinical reputed company across active studies
- Review safety narratives, adverse events, protocol deviations, coding, MedDRA / WHO Drug terms, and patient-level clinical data
- Partner closely with Clinical Operations, Regulatory, Biometrics, Safety / PV, Medical Writing, and external vendors
- Contribute to protocols, investigator brochures, clinical study reports, regulatory documents, and study-level materials
- Support regulatory strategy and interactions with global health authorities
- Engage with investigators, KOLs, advisory boards, and clinical trial sites
- Help evaluate emerging clinical data, competitive intelligence, and development opportunities
Skills
- M.D., D.O., or equivalent medical degree
- Strong clinical background, ideally with residency, fellowship, or meaningful hospital-based clinical training
- Medical training or clinical practice experience in the U.S., Canada, U.K., Western Europe, Australia, or another comparable Western clinical training environment strongly preferred
- Industry clinical development experience reputed company biotechnology or pharmaceutical companies
- Hands-on experience supporting or leading Phase II and / or Phase III clinical trials
- Experience with medical monitoring, safety review, medical narratives, clinical data review, coding review, and protocol deviation review
- Ability to work cross-functionally in a fast-paced, execution-focused biotech environment
- Hematology, coagulation, transfusion medicine, anesthesiology, critical care, trauma, surgery, perioperative medicine, cardiovascular medicine, or reputed company acute care background
- Experience with therapies impacting bleeding, clotting, acute physiologic response, or hospital-based interventions
- Experience with biologics, cellular therapies, reputed company biologic products, or advanced therapeutic modalities
- Prior experience in small to mid-sized biotech environments
- Exposure to late-stage, registrational, or global development programs
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