VP of Clinical Operations

Barrington James; Lyon; Hybride; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A clinical operations leadership firm is seeking a Vice President of Clinical Operations to oversee global clinical trial execution and operational strategy. The role demands at least 10 years of experience in clinical operations and strong leadership skills. The ideal candidate will have a deep understanding of regulatory compliance, a proven track record in managing large teams, and experience with global clinical studies. This position offers competitive compensation and a hybrid work model.

Prestations

Competitive executive compensation

Health, dental, vision, and life insurance

Equity or stock option opportunities

Generous PTO

Flexible work environment

Professional development support

Qualifications

• 10+ years of experience in clinical operations in a CRO, biotech, or pharmaceutical company.
• 5+ years in a senior leadership role overseeing clinical trial execution.
• Strong knowledge of ICH-GCP, FDA, EMA regulations.
• Proven success in leading global clinical studies and managing large teams.
• Excellent strategic thinking and organizational skills.

Responsabilités

• Lead global clinical trial execution from planning to closeout.
• Develop clinical operations strategy and manage budgets.
• Mentor clinical operations teams and collaborate with sponsors.
• Drive continuous improvement initiatives and manage vendors.
• Support regulatory submissions and track KPIs.

Connaissances

Leadership

Strategic planning

Clinical trial management

Communication

Organizational skills

Formation

Bachelor's degree in Life Sciences, Nursing, Pharmacy

Master’s or advanced degree (MS, MBA, MPH) preferred

Outils

eTMF

EDC

CTMS

eCOA

IRT

Description du poste

VP of Clinical Operations Role :

Location : Europe Based, Any

Department : Clinical Operations

Type : Hybrid

Position Summary :

The Vice President of Clinical Operations is responsible for the strategic oversight and operational execution of clinical trials across all phases (I–IV). This role leads cross-functional teams to ensure the efficient, high-quality, and compliant delivery of clinical programs in alignment with corporate goals and regulatory requirements. As a senior leader within the organisation, the VP of Clinical Operations plays a critical role in sponsor engagement, resource planning, and operational excellence.

Key Responsibilities :

• Lead and oversee all aspects of global clinical trial execution including planning, startup, enrolment, site management, data collection, and closeout.
• Develop and implement clinical operations strategy to ensure successful delivery of clinical programs on time and within budget.
• Manage and mentor clinical operations teams including Clinical Trial Managers (CTMs), Clinical Research Associates (CRAs), and support staff.
• Serve as a key liaison with sponsors, investigators, regulatory bodies, and internal cross-functional teams (e.g., regulatory, data management, biostats).
• Ensure trials are conducted in accordance with ICH-GCP, FDA / EMA regulations, and internal SOPs.
• Collaborate with executive leadership to define timelines, budgets, risk mitigation plans, and resource allocation.
• Drive continuous improvement initiatives related to clinical processes, vendor performance, quality control, and patient recruitment strategies.
• Evaluate, select, and manage vendors such as CROs, central labs, and eClinical platforms.
• Support regulatory submissions and inspection readiness activities.
• Develop and track KPIs across the clinical portfolio to ensure operational excellence.

Qualifications :

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field; Master’s or advanced degree (MS, MBA, MPH) preferred.

Minimum 10 years of experience in clinical operations within a CRO, biotech, or pharmaceutical company.

At least 5 years in a senior leadership role with direct oversight of clinical trial execution and team leadership.

Strong working knowledge of ICH-GCP, FDA, EMA, and other international clinical trial regulations.

Proven success in leading multi-centre, global clinical studies from startup to closeout.

Experience managing large teams and clinical budgets.

Excellent organizational, communication, and strategic thinking skills.

Demonstrated ability to manage multiple projects and shifting priorities in a fast-paced environment.

Preferred Experience :

Experience with electronic clinical systems (eTMF, EDC, CTMS, eCOA, IRT, etc.).

Familiarity with oncology, rare disease, CNS, or other complex therapeutic areas.

Prior involvement in regulatory submissions (IND, NDA, BLA) is a plus.

Experience working with decentralized / hybrid trial models is desirable

Compensation & Benefits :

Competitive executive compensation with performance-based incentives

Health, dental, vision, and life insurance

Equity or stock option opportunities (for biotech / pharma)

Competitive salary

Generous PTO and flexible work environment

Professional development and leadership training support

This opportunity has been incredibly popular. We encourage all candidates to apply immediately, as it is likely that recruitment may close prematurely.