Clinical Development Lead

Randstad · Burgess Hill, South East

Clinical Development Lead at Randstad, based in Burgess Hill, South East. This is a contract role with hybrid working.

Salary
Competitive
Location
Burgess Hill, South East · Hybrid
Contract
Contract
Posted
3 days ago
Closes
27 Oct 2026
Sector
Regulatory Affairs

Reference PR-1550251

About the role

Clinical Development Lead - Cardiovascular & Metabolic Diseases (CVMD)

Location: Burgess Hill, UK (Hybrid: Up to 2 days per week on-site)

Contract Duration: 6 Months

Are you a senior clinical development expert with a strong background in Cardiovascular and Metabolic Diseases? We are seeking a high-calibre Clinical Development Lead to join a global diagnostic leader driving innovation in early diagnosis and personalised medicine.


The Role

In this senior strategic role, you will lead complex clinical development programs for next-generation diagnostic solutions within CVMD. Operating as a trusted medical authority, you will define clinical utility, oversee large-scale studies, and drive competitive differentiation across the portfolio.


Key Responsibilities
  • Drive Clinical Strategy: Lead clinical development activities, study designs, and portfolio strategy for CVMD diagnostic programs.
  • Regulatory Leadership: Partner with Global Regulatory Affairs to author critical submission packages for health authority filings globally.
  • Stakeholder Engagement: Serve as the medical lead for external health authority interactions and build strategic partnerships with global Key Opinion Leaders (KOLs), industry, and academia.
  • Scientific Communication: Oversee trial communication strategies, presenting at global medical congresses and driving key scientific publications.
  • Mentorship & Pipeline Support: Support intellectual property strategies, early pipeline activities, and mentor team members across the department.

What We Are Looking For
  • Education: Medical degree (MD) or PhD in cardiology, metabolic diseases, obesity, or a related discipline.
  • Industry & Trial Experience: Proven track record in In Vitro Diagnostics (IVD) or Medical Devices across all stages of global clinical trials, including protocol design and report writing.
  • Regulatory Standards: In-depth knowledge of international regulatory frameworks and guidelines (ICH-GCP, IVDD/IVDR, MDR, FDA, NMPA).
  • Leadership: Strong cross-functional program leadership skills within complex matrix environments.
  • Mobility: Willingness to travel up to 25% depending on project phases.

Randstad Business Support is acting as an Employment Business in relation to this vacancy.

Reference: PR-1550251 · Posted 3 days ago · Closes 27 Oct 2026 · Listed via Randstad

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