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VP of Medical (Clinical Development)

VP of Medical (Clinical Development)

Reference: BBBH28970
Date posted: 02/04/2026
Job details
Specialism
Clinical Development
Expertise
Clinical Scientist
Location
Frankfurt, Hessen, Germany
Job type
Permanent
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Description

Are you ready to shape the future of clinical development by leading the medical and scientific vision behind breakthrough clinical trials?

R&D Partners is seeking a Vice President, Medical to lead the medical, scientific, and strategic aspects of clinical trials. In this role, you will oversee the planning, execution, and reporting of clinical studies, ensuring compliance with regulatory standards. You will also contribute to the development of clinical strategies, collaborate with cross-functional teams, and act as a key liaison with regulatory authorities and external stakeholders. This position does require a 3-4 day visit to the office once a month.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Develop clinical plans for early-stage drug trials, including First-in-Human (FiH) and Proof-of-Concept (PoC) strategies.
  • Create and review essential documents such as study protocols, reports, investigator brochures, and regulatory submissions.
  • Provide medical expertise to clinical operations and cross-functional teams.
  • Collaborate with service providers, including CROs and laboratories, to ensure quality and compliance.
  • Offer medical-scientific input on business strategies, licensing activities, and project plans.
  • Build relationships with key opinion leaders and academic institutions.
  • Oversee safety monitoring, data review, and compliance with ICH-GCP guidelines.
  • Support regulatory meetings and interactions with authorities like EMA and FDA.
  • Develop and approve training materials for internal and external stakeholders.

Key Skills and Requirements:

  • Medical degree with experience in clinical research.
  • Background in oncology or hematology, or relevant drug development experience in these areas.
  • Knowledge of clinical drug development, pharmacovigilance, biostatistics, and GCP guidelines.
  • Familiarity with regulatory processes and authorities (e.g., EMA, FDA) is a plus.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to work independently and collaboratively in team settings.
  • Proficiency in English for both medical and business contexts.

For more information, please contact Calum Watson.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

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Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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