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Vp Clinical Development Jobs (NOW HIRING)

Reporting to the Global Head of Oncology Clinical Development, the Vice President, Oncology, Clinical Development will play a pivotal leadership role during a period of significant organizational ...

Reporting to the Global Head of Oncology Clinical Development, the Vice President, Oncology, Clinical Development will play a pivotal leadership role during a period of significant organizational ...

The Vice President will drive the strategies and clinical plans across all phases of drug development. Key domains include development of study protocols, medical review of clinical trial data, and ...

Position Overview The Vice President (VP), Clinical Development - Infectious Disease is a leadership role responsible for guiding Tonix Pharmaceuticals' clinical development programs. Reporting ...

Along with this, the SVP of Clinical Development will support and build the clinical development team which includes medical leads, medical directors, and clinical research scientists who will be ...

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Vp Clinical Development information

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$62K

$160.6K

$263.5K

How much do vp clinical development jobs pay per year?

As of Jul 6, 2026, the average yearly pay for vp clinical development in the United States is $160,591.00, according to ZipRecruiter salary data. Most workers in this role earn between $119,000.00 and $193,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a VP of Clinical Development, and why are they important?

To thrive as a VP of Clinical Development, you need deep expertise in clinical research, drug development, and regulatory affairs, typically supported by an advanced degree in medicine, pharmacy, or life sciences. Familiarity with clinical trial management systems (CTMS), data analysis tools, and current Good Clinical Practice (GCP) guidelines is essential, along with certifications such as PMP or RAC being advantageous. Strong leadership, strategic thinking, and excellent communication skills set outstanding candidates apart in this role. These skills ensure effective oversight of clinical programs, regulatory compliance, and successful collaboration across multidisciplinary teams to drive product development.

What does a VP of Clinical Development do?

A VP of Clinical Development oversees the planning, management, and execution of clinical trials for new drugs or medical devices within a pharmaceutical or biotech company. They lead teams that design clinical studies, ensure regulatory compliance, and analyze trial data to support product approval. This role also involves collaborating with cross-functional teams, managing budgets, and representing the company to regulatory agencies. Their work is critical in bringing safe and effective therapies to market.

What are the primary challenges a VP of Clinical Development faces when leading cross-functional teams in clinical trials?

A VP of Clinical Development often manages diverse teams that include clinical operations, regulatory affairs, data management, and medical affairs. One key challenge is ensuring clear communication and alignment across these functions, especially as clinical trials grow in complexity and scale. Balancing strategic oversight with hands-on problem-solving is essential, particularly when addressing regulatory changes or unanticipated trial issues. Effective collaboration and proactive leadership are crucial to maintaining timelines, budget, and data quality throughout the development process.

What is the difference between Vp Clinical Development vs Clinical Operations Manager?

AspectVp Clinical DevelopmentClinical Operations Manager
Required CredentialsAdvanced degrees (PhD, MD, or PharmD), extensive industry experienceBachelor's or Master's in life sciences, relevant experience in clinical trials
Work EnvironmentStrategic leadership, cross-functional collaboration, executive meetingsOperational oversight, site management, trial coordination
Employer & Industry UsagePharmaceutical, biotech companies, CROs at senior levelsClinical trial sites, biotech firms, pharmaceutical companies

The Vp Clinical Development focuses on strategic planning, clinical trial design, and regulatory strategy at an executive level. In contrast, the Clinical Operations Manager handles day-to-day trial execution, site management, and operational logistics. Both roles are essential in clinical research but differ in scope, responsibilities, and seniority.

More about Vp Clinical Development jobs
What cities are hiring for Vp Clinical Development jobs? Cities with the most Vp Clinical Development job openings:
What are the most commonly searched types of Clinical Development jobs? The most popular types of Clinical Development jobs are:
What states have the most Vp Clinical Development jobs? States with the most job openings for Vp Clinical Development jobs include:
Infographic showing various Vp Clinical Development job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 3% As Needed, 8% Full Time, 87% Part Time, and 1% Temporary. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $160,591 per year, or $77.2 per hour.

Vice President, Clinical Development

Servier

Boston, MA โ€ข Hybrid

Other

Medical, Dental, Vision, Life, Retirement

This job post hasย expired today.ย Applications are no longer accepted.


Job description

About Servier

Servier in the U.S. is a Boston-based, commercial-stage biopharmaceutical organization launched by the Servier Group in 2018. As a privately held, patientfocused company, Servier is uniquely positioned to pursue innovative science, accelerate transformative therapies, and advance treatments in underserved areas of oncology. Our agile structure and global footprint enable us to make bold strategic decisions in service of patients worldwide.

Role Summary

Servier is seeking a highly experienced and visionary clinical development leader to join its global Oncology Clinical Development Leadership Team. Reporting to the Global Head of Oncology Clinical Development, the Vice President, Oncology, Clinical Development will play a pivotal leadership role during a period of significant organizational growth and transformation.

The Vice President will provide enterprise-level leadership for a substantial portion of Servier's oncology portfolio within an evolving, integrated development model. Programs may transition responsibility at Proof of Clinical Concept (POCC) or be advanced seamlessly from firstinhuman (FIH) through registration. In addition to portfolio leadership, this role carries shared accountability for defining, directing, and continuously improving the scientific strategy, operating model, and performance of the global oncology development organization.

This role is expected to assume delegated authority for selected global and enterprise responsibilities from the Global Head of Oncology Clinical Development, requiring seasoned judgment, operational maturity, and the ability to drive complex decision-making in a highly matrixed environment.

Key Responsibilities

Enterprise & Strategic Leadership

  • Direct clinical development strategy for a significant portion of the oncology portfolio, with primary focus on adult solid tumors and strategic input across the broader oncology pipeline.
  • Serve as a core member of the Oncology Clinical Development Leadership Team with joint responsibility for portfolio prioritization, business development advice, and development governance.
  • Represent Oncology Clinical Development at senior global governance forums and act as a designated delegate for the Global Head in executive decision-making bodies, as appropriate.
  • Provide enterprise-level leadership in areas such as operational excellence, portfolio-wide development standards, and continuous improvement of decision-making frameworks.

Clinical Development Excellence

  • Provide executive oversight for end-to-end clinical development programs, from early clinical planning through latestage development, registration, and lifecycle management.
  • Ensure high scientific and ethical standards across all clinical activities, including protocol design, safety oversight, data interpretation, and regulatory submissions.
  • Apply seasoned clinical judgment to complex program, portfolio, and risk-benefit decisions at key development inflection points.

Cross-Functional & Global Collaboration

  • Lead effectively within a highly matrixed, global organization, partnering across research, translational medicine, regulatory, safety, operations, commercial, and alliance teams.
  • Drive alignment and continuity across early and late development activities, supporting Servier's integrated oncology development model.
  • Build strong partnerships with global key opinion leaders, academic investigators, and external collaborators to support strategic objectives.

Organizational Leadership & Capability Building

  • Lead and develop senior clinical development leaders, physicians, and scientists, with accountability for building sustainable organizational capability and succession.
  • Set expectations and standards for leadership behaviors, talent development, and scientific excellence across the global clinical organization.
  • Contribute to broader enterprise initiatives focused on leadership development, organizational effectiveness, and culture.

Education & Required Experience

  • M.D. or equivalent medical degree.
  • Board Certification or Eligibility in Oncology (Medical Oncology preferred).
  • 12+ years of progressive experience in oncology drug development with 5+ years in mid-large pharma, including substantial late-stage and registrational leadership.
  • Demonstrated track record of enterprise-level leadership, sound clinical judgment, and effective decision-making across complex portfolios.
  • Deep expertise in adult solid tumors; broader oncology experience, including hematologic malignancies, is desirable.
  • Proven success operating in a global, highly matrixed environment with significant cross-functional influence.
  • Experience representing clinical development at senior governance forums and engaging with health authorities is strongly preferred.

Travel & Location

  • Up to 20% travel (domestic and international).
  • Boston-based hybrid role (2-3 days/week in the Boston Seaport office).

Servier's Commitment

Servier is committed to fostering an environment of diversity, equity, and inclusion. We welcome applicants who are passionate, experienced, and innovative-even if their background doesn't perfectly match every qualification listed.

All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Job Description
Candidate Profile

Salary Range

The salary range for this role is $342,000 - $433,000. An employee's pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Employees in this position are also eligible for Short-Term and Long-Term incentive programs.ย Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements).ย  For more information on our benefits, please visit this link.