Clinical Development Medical Director (CDMD)

Posted 1 day 12 hours ago by Barrington James Limited

£125,000 - £150,000 Annual
Permanent
Full Time
Other
London, United Kingdom
Job Description
Clinical Development Medical Director (CDMD)

Barrington James has partnered with a leading pharmaceutical corporation. Looking for a highly رؤ 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 hermoso 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.

If you have a passion for clinical advancement, join a top tier pharma company and make an impact on the future of drug development. Apply now!