Clinical Development Medical Director (CDMD)
50239
Posted: 14/01/2026
- London , United Kingdom
- Permanent
Clinical Development Medical Director (CDMD)
Job Overview:
Barrington James has partnered with a leading pharmaceutical corporation. Looking for a highly experienced and strategic Clinical Development Medical Director (CDMD) to lead and manage the clinical development of leading-edge programs that aim to make a significant impact on patient care. Your responsibilities will entail overseeing all phases of clinical development for assigned programs and being a part of a collaborative and agile environment.
Key Responsibilities:
Qualifications and Experiences:
Job Overview:
Barrington James has partnered with a leading pharmaceutical corporation. Looking for a highly experienced and strategic Clinical Development Medical Director (CDMD) to lead and manage the clinical development of leading-edge programs that aim to make a significant impact on patient care. Your responsibilities will entail overseeing all phases of clinical development for assigned programs and being a part of a collaborative and agile environment.
Key Responsibilities:
- Lead and provide medical expertise for all aspects of clinical objectives within a project.
- Oversee the creation and development of regulatory documents at the trial and program levels.
- Execution of clinical programs and trials, working alongside global teams and medical professionals to ensure milestones are met.
- Support the senior leadership team in maintaining the overall safety profile of the product, collaborating with safety and clinical operations teams.
- Contribute medical insights to the development of clinical strategies, protocols, and plans, ensuring alignment with overall therapeutic goals.
- Serve as a key medical liaison in discussions with both internal and external stakeholders, helping guide decision-making at various levels.
- Collaborate with research teams and other departments to lead projects from early-phase research to full clinical development.
Qualifications and Experiences:
- MD / or similar medical background with advanced medical training.
- Strong clinical background, with board certification including experience from residency/fellowship.
- Prior experience in clinical research / pharmaceutical development is highly desirable.
- Proven expertise in clinical trial management across Phases I-IV, with hands-on experience in trial design, execution, and reporting.
- Thorough knowledge of the clinical development processes, statistical analysis, regulatory guidelines (GCP).
- In-depth understanding of disease areas, clinical data analysis, and research reports.
- Ability to work effectively with cross-functional teams and build strong scientific partnerships.
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