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Vice President Clinical Development Jobs (NOW HIRING)

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 ...

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Vice President Clinical Development information

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$62K

$160.6K

$263.5K

How much do vice president clinical development jobs pay per year?

As of Jul 6, 2026, the average yearly pay for vice president 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 does a Vice President of Clinical Development do?

A Vice President of Clinical Development is responsible for overseeing the planning, execution, and management of clinical trials and research activities within a pharmaceutical or biotechnology company. They lead teams that design clinical study protocols, ensure compliance with regulatory standards, and collaborate with cross-functional departments to advance drug candidates from early development through to approval. This role also involves strategic input into product development, budget management, and fostering relationships with external partners such as clinical research organizations and regulatory agencies. Their leadership is crucial to ensuring that clinical programs are scientifically sound, ethically conducted, and aligned with company goals.

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

To thrive as a Vice President Clinical Development, you need extensive experience in clinical research, a strong background in medicine or life sciences (often with an MD or PhD), and proven leadership in drug development. Familiarity with regulatory requirements, clinical trial management systems, and certifications such as GCP (Good Clinical Practice) are typically necessary. Exceptional communication, strategic thinking, and cross-functional team leadership distinguish top performers in this role. These skills are crucial for successfully guiding clinical programs, ensuring regulatory compliance, and driving innovation in pharmaceutical development.

What are the main challenges faced by a Vice President of Clinical Development when overseeing multiple clinical trials simultaneously?

A Vice President of Clinical Development often manages several clinical trials at different phases, which can present challenges such as balancing timelines, budgets, and regulatory requirements across projects. Coordinating cross-functional teams—including clinical operations, regulatory affairs, and data management—requires strong communication and organizational skills. Additionally, adapting to evolving scientific data and ensuring compliance with global regulations are ongoing demands. Success in this role often depends on the ability to make strategic decisions quickly while maintaining the highest standards of patient safety and data integrity.

What is the difference between Vice President Clinical Development vs Director of Clinical Development?

AspectVice President Clinical DevelopmentDirector of Clinical Development
ResponsibilitiesOversees entire clinical development strategy, manages senior teams, and interacts with executive leadershipManages clinical trial operations, oversees project teams, and ensures trial compliance
Required CredentialsAdvanced degree (MD, PhD, or PharmD), extensive industry experience, leadership skillsRelevant degree (MD, PhD, or PharmD), clinical trial experience, project management skills
Work EnvironmentStrategic planning, cross-department collaboration, high-level decision makingOperational focus, team management, trial execution oversight

The Vice President Clinical Development typically holds a higher strategic and leadership role, overseeing the entire clinical development process and interacting with executive teams. The Director of Clinical Development focuses more on managing clinical trials and operational activities. Both roles require relevant advanced degrees and industry experience, but the VP position emphasizes strategic oversight and leadership.

What cities are hiring for Vice President Clinical Development jobs? Cities with the most Vice President 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 Vice President Clinical Development jobs? States with the most job openings for Vice President Clinical Development jobs include:
Infographic showing various Vice President Clinical Development job openings in the United States as of June 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $160,591 per year, or $77.2 per hour.

Vice President, Clinical Development

Servier

Boston, MA • Hybrid

Other

Medical, Dental, Vision, Life, Retirement

This job post has expired today. 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. 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).  For more information on our benefits, please visit this link.