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Contract Clinical Project Manager Jobs (NOW HIRING)

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech ...

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech ...

Company Description PSI is a leading Contract Research Organization with 30 years in the industry ... full-service clinical research projects in phase II and III, managing the full scope of ...

Clinical Project Management is focused on project delivery, productivity and quality resulting in ... Monitor progress against contract and prepare/present project and/or sub-team information ...

Clinical Project Management is focused on project delivery, productivity and quality resulting in ... against contract and prepare/present project and/or sub-team information proactively to ...

Experience managing clinical research projects involving investigational products within a Contract Research Organization (CRO) or pharmaceutical environment. * Clinical trial experience and ...

Experience managing clinical research projects involving investigational products within a Contract Research Organization (CRO) or pharmaceutical environment. * Clinical trial experience and ...

Job Summary Clinical Project Manager (CPM) is key to the success of the overall conduct of a ... Support vendor selection process, including RFP to contract and change order process for CROs and ...

Clinical Project Manager

Novato, CA · On-site

$90K - $100K/yr

The Clinical Project Manager will oversee study operations, staff, regulatory compliance, data and biospecimen quality, timelines, budgets, and coordination with internal and external stakeholders.

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How much do contract clinical project manager jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for contract clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

What is a contract clinical project manager?

A Contract Clinical Project Manager oversees the planning, execution, and completion of clinical trials on a contract basis, typically for pharmaceutical or biotech companies. They ensure studies adhere to regulatory requirements, timelines, and budgets while coordinating cross-functional teams. Unlike permanent roles, contract positions are temporary and project-specific, offering flexibility and diverse experience across multiple organizations.

What are the key skills and qualifications needed to thrive in the contract clinical project manager position, and why are they important?

To thrive as a Contract Clinical Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and certifications such as PMP or CCRA are highly valued. Exceptional organizational, leadership, and cross-functional communication skills help manage timelines, stakeholders, and remote project teams effectively. These competencies ensure studies are delivered on schedule, within budget, and in accordance with regulatory standards.

What are the typical challenges faced by contract clinical project managers, and how can they be addressed?

Contract Clinical Project Managers often navigate challenges such as balancing tight project timelines, ensuring compliance across multiple sites, and managing cross-functional teams with varying priorities. Adaptability and strong organizational skills are crucial for quickly resolving issues, reallocating resources, and maintaining clear communication between sponsors, CROs, and site staff. Proactive risk management, regular status reporting, and agile project adjustments can significantly streamline workflow and mitigate setbacks. By building collaborative relationships and fostering open communication, project managers can more efficiently address emerging challenges and keep clinical trials on track.

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Infographic showing various Contract Clinical Project Manager job openings in the United States as of September 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Project Manager

Baltimore, MD

Pharmaron
Chemical Manufacturing • 10K+ employees

$80K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

Position: Clinical Project Manager

Salary Range: $80K-$135K

Location: Baltimore, MD

Unfortunately, we cannot support work visa permit applications for this role

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

Job Overview:

The Clinical Project Manager (CPM) is the single, accountable leader for early-phase (FIH, SAD/MAD, food-effect, DDI, 14C etc.) clinical trials, translating Sponsor protocols into integrated project plans and guiding cross-functional teams from study initiation and first-subject-in through CSR submission and TMF delivery. Acting as the primary interface for Sponsors, investigators, vendors, and senior leadership, the CPM governs study scope, timelines, budgets, and risk, ensuring ICH-GCP and global regulatory compliance while protecting project margin through rigorous change-order and vendor oversight. Leveraging real-time dashboards and eClinical systems, the CPM drives proactive issue resolution, produces executive-level status reports, and maintains inspection-ready documentation. Success is defined by on-time, on-budget delivery of high-quality data, exemplary Sponsor satisfaction, and continuous process improvement that elevates PM Department and clinical unit performance.

Key Responsibilities:

  • Partner with Business Development to support feasibility assessments and site qualification activities
  • Collaborate with regulatory teams to ensure accurate and complete feasibility documentation
  • Build strong sponsor relationships by understanding client needs and ensuring confidence in study execution
  • Contribute to proposal development, including cost estimation and preparation of sponsor-ready submissions
  • Lead project kick-off meetings and align cross-functional teams and external stakeholders
  • Coordinate with vendors and consultants to define scope, timelines, and deliverables
  • Develop and manage project timelines, proactively identifying risks and implementing mitigation strategies
  • Serve as the primary point of contact for sponsors, ensuring clear communication and on-time delivery
  • Monitor project progress, budgets, and performance metrics; analyze trends and address issues proactively
  • Review financials, approve vendor expenses, and partner with Project Finance on scope and budget changes
  • Ensure high-quality study closeout deliverables, respond to sponsor inquiries, and lead lessons learned for continuous improvement

What We're looking for Clinical Project Manager:

  • CPM: Associates / equivalency (60 or more college credit hours) in related field + 2 years as a Project Manager; OR Bachelor of Science in related field + 1 year as a Project Manager. 3 years of Project Management experience in a Clinical Research environment may be substituted for educational requirements.
  • CPM: Bachelor of Science in related field + 2 year as a Project Manager Clinical Research environment preferred.

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits:

As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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