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Director Clinical Project Management information

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$124.4K

$183K

How much do director clinical project management jobs pay per year?

As of Jul 28, 2026, the average yearly pay for director clinical project management in the United States is $124,379.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,000.00 and $147,500.00 per year, depending on experience, location, and employer.

What does a Director of Clinical Project Management do?

A Director of Clinical Project Management oversees the planning, execution, and completion of clinical trials within a pharmaceutical or biotech company. They lead project management teams, ensure regulatory compliance, manage budgets and timelines, and coordinate communication among stakeholders. Their responsibilities also include risk management, resource allocation, and ensuring trials meet both scientific and business objectives. This role is critical for bringing new medical treatments through the development pipeline to market approval.

What are the key skills and qualifications needed to thrive as a Director of Clinical Project Management, and why are they important?

To thrive as a Director of Clinical Project Management, you need deep expertise in clinical research, regulatory compliance, project leadership, and typically an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or CCRP are commonly required. Strong strategic thinking, communication, and team leadership skills help drive project success and foster collaboration among cross-functional teams. These competencies are vital for delivering clinical trials on time, within budget, and in compliance with regulatory standards.

What is the difference between Director Clinical Project Management vs Clinical Project Manager?

AspectDirector Clinical Project ManagementClinical Project Manager
ResponsibilitiesOversees multiple projects, strategic planning, team leadershipManages individual clinical trials, day-to-day operations
Experience & CredentialsTypically requires 8+ years, advanced degrees, leadership experienceUsually 3-5 years, relevant clinical or project management certifications
Work EnvironmentSenior management, cross-functional teams, strategic meetingsProject teams, site coordination, operational tasks

The main difference is that the Director Clinical Project Management holds a senior leadership role overseeing multiple projects and strategic initiatives, while the Clinical Project Manager focuses on managing individual clinical trials and operational activities. Both roles require relevant experience and certifications, but the director's scope is broader and more strategic.

What are some common challenges faced by a Director of Clinical Project Management, and how can they be addressed?

Directors of Clinical Project Management often encounter challenges such as managing complex, multi-site trials, maintaining regulatory compliance, and coordinating cross-functional teams. Balancing timelines, budgets, and quality expectations can also be demanding, especially when unexpected issues arise. Successful directors address these challenges by fostering clear communication, utilizing robust project management tools, and building strong relationships with stakeholders. Staying current with regulatory changes and providing mentorship to team members also helps ensure project success and professional growth.
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Director Clinical Project Management jobs near you
Infographic showing various Director Clinical Project Management job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $124,379 per year, or $59.8 per hour.
Global Director, Clinical Project Management

Global Director, Clinical Project Management

Systimmune

Princeton, NJ • On-site

$180K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
We are seeking a highly skilled and motivated Global Director, Clinical Project Management (CPM) to join our dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders.  The global Director, Clinical Project Management will play a critical role in delivering high-quality data and ensuring the success of clinical studies.
This position requires onsite hybrid work model in Princeton, NJ. 
Responsibilities
  • Oversee the planning and execution of global clinical trials
  • Develop and implement study protocols, timelines, and budgets.
  • Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout.
  • Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
  • Coordinate with cross-functional teams, including investigators, vendors, and regulatory bodies.
  • Monitor trial progress and manage data collection to ensure accuracy and integrity.
  • Identify and mitigate project risks
  • Oversee a team of regional CPMs, CRAs and CTAs.
  • Ensure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practice.
  • Conduct regular meetings with study teams and provide updates to stakeholders.
  • Coordinate with external vendors and partners involved in the trial
  • Support development of key process initiatives and SOPs internally
  • Oversee vendors supporting trial execution

Qualifications
  • Bachelor’s degree in Life Sciences, Nursing, or a related field.
  • Minimum of 10 years of experience in clinical trial management, including at least 5 years in a direct line management role.
  • Strong understanding of GCP and regulatory requirements.
  • Excellent organizational and project management skills.
  • Proven ability to lead cross-functional teams and manage multiple priorities.
  • Strong communication and interpersonal skills.
  • Ability to work collaboratively in a team-oriented environment
  • Flexibility and adaptability to changing priorities and workload
  • Master’s degree in a related field or clinical research certification (e.g., ACRP or SOCRA).
  • Experience with electronic data capture (EDC) systems and clinical trial management software.
  • Prior experience in running or supporting Oncology clinical trials a plus.
  • Previous experience in a sponsor or CRO environment.
Location/Travel:
  • Princeton NJ onsite in office
  • Overnight travel ~25%

Compensation and Benefits:
The expected base salary range for this position is $180,000 - $230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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