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Open nowPosted 139 days ago

VP, Clinical Operations and Data Management

Workable (global search)108,016 open roles

Where
London, England, United Kingdom
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Your applicationOpen nowVP, Clinical Operations and Data ManagementWorkable (global search) · London, England, United Kingdom

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The clock on this job

Early applications get read.

7.9% of postings close within 7 days. Measured by our own scanner across the market. Workable (global search) postings stay open a median of 7 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.6%3 days
  3. 7.9%7 days
  4. 14.9%14 days
  5. 34.0%30 days
This job: posted 139 days ago

Workable (global search) median: 7 days open

The posting

Reporting to: Chief Medical Officer

Location: London

Job Summary

The Vice President of Clinical Operations and Data Management (CODM) provides strategic leadership for the planning, execution, and oversight of global clinical trials. This role is accountable for delivering high-quality, compliant, patient-focused studies on time and within budget, while advancing the organization’s clinical development strategy and supporting global regulatory and commercialization objectives.

Key Elements and Responsibilities

· Provide strategic and operational leadership for clinical operations and data management across programs, from study start-up through close-out, in compliance with ICH-GCP.

· Ensure the quality, integrity, and inspection-readiness of all clinical and data management activities globally.

· Drive cross-functional collaboration to deliver clinical trials on time and within budget.

· Lead planning, execution, and reporting of clinical studies, ensuring alignment on timelines, deliverables, and resources.

· Act as the primary escalation point for critical study and vendor issues.

· Oversee study budgets, timelines, resources, and financial tracking.

· Partner with Clinical Science, Biostatistics, and external vendors to ensure seamless delivery of:

o Clinical documentation

o Data management activities

· Ensure effective coordination of regulatory submissions (e.g., IRB/ethics committees, local authorities).

· Oversee data management strategy and execution, including database design, build, maintenance, and database lock activities, in alignment with biostatistics.

· Ensure robust data integrity, accurate record-keeping, and compliant archiving practices.

· Provide oversight of clinical sites, academic partners, and vendors (e.g., CROs, labs) to ensure performance, quality, and compliance.

· Build and maintain strong relationships with investigators and key opinion leaders.

· Lead, develop, and mentor high-performing teams.

· Ensure delivery of high-quality study documentation to meet program timelines.

Requirements

Experience, Skills & Knowledge

· Extensive experience in clinical operations leadership within biotech/pharma.

· Strong clinical project and program management expertise.

· Proven track record managing CROs and external vendors.

· Solid understanding of global regulatory requirements (ICH-GCP).

· Experience managing budgets and resource planning.

· Strong problem-solving skills with the ability to operate strategically and tactically.

· Excellent leadership, communication, and stakeholder management skills.

· Ability to thrive in a fast-paced, evolving biotech environment.

· Experience in rare/orphan diseases and/or academic collaborations is a plus.

Education

  • Bachelor’s degree in Life Sciences required.
  • Advanced degree (MS, PhD, or equivalent) preferred.
  • Substantial experience leading Clinical Operations and Data Management teams.

· Experience in rare disease; gene and cell therapy experience is a plus

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