VP, Clinical Operations and Data Management
Podsumowanie roli od JobGrid
VP, Clinical Operations and Data Management at Orchard Therapeutics: London, Wielka Brytania; Hybrydowo; Opieka zdrowotna i nauka. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.
- Location and workplace: London, Wielka Brytania, Hybrydowo
- Role classification: Opieka zdrowotna i nauka
- Source freshness: checked by JobGrid on 2026-05-29.
- Application path: candidates continue to the employer application page with non-personal referral tags.
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鈥檚 clinical development strategy and supporting global regulatory and commercialization objectives.
Key Elements and Responsibilities
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路聽聽聽聽聽聽聽聽 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.
路聽聽聽聽聽聽聽聽 Ensure the quality, integrity, and inspection-readiness of all clinical and data management activities globally.
路聽聽聽聽聽聽聽聽 Drive cross-functional collaboration to deliver clinical trials on time and within budget.
路聽聽聽聽聽聽聽聽 Lead planning, execution, and reporting of clinical studies, ensuring alignment on timelines, deliverables, and resources.
路聽聽聽聽聽聽聽聽 Act as the primary escalation point for critical study and vendor issues.
路聽聽聽聽聽聽聽聽 Oversee study budgets, timelines, resources, and financial tracking.
路聽聽聽聽聽聽聽聽 Partner with Clinical Science, Biostatistics, and external vendors to ensure seamless delivery of:
o聽聽 Clinical documentation
o聽聽 Data management activities
路聽聽聽聽聽聽聽聽 Ensure effective coordination of regulatory submissions (e.g., IRB/ethics committees, local authorities).
路聽聽聽聽聽聽聽聽 Oversee data management strategy and execution, including database design, build, maintenance, and database lock activities, in alignment with biostatistics.
路聽聽聽聽聽聽聽聽 Ensure robust data integrity, accurate record-keeping, and compliant archiving practices.
路聽聽聽聽聽聽聽聽 Provide oversight of clinical sites, academic partners, and vendors (e.g., CROs, labs) to ensure performance, quality, and compliance.
路聽聽聽聽聽聽聽聽 Build and maintain strong relationships with investigators and key opinion leaders.
路聽聽聽聽聽聽聽聽 Lead, develop, and mentor high-performing teams.
路聽聽聽聽聽聽聽聽 Ensure delivery of high-quality study documentation to meet program timelines.