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Clinical Project Leader Jobs (NOW HIRING)

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

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 ...

As a Clinical Project Manager, you will play a critical role in leading cross-functional clinical projects, driving operational excellence, and ensuring successful study execution from start-up ...

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

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 ...

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

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 ...

As a Clinical Project Manager, you will play a critical role in leading cross-functional clinical projects, driving operational excellence, and ensuring successful study execution from start-up ...

As a Clinical Project Manager, you will play a critical role in leading cross-functional clinical projects, driving operational excellence, and ensuring successful study execution from start-up ...

CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical aspects of a trial within contractual and budgetary requirements. The CTL oversees the ...

CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical aspects of a trial within contractual and budgetary requirements. The CTL oversees the ...

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Clinical Project Leader information

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$63

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How much do clinical project leader jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical project leader in the United States is $63.00, according to ZipRecruiter salary data. Most workers in this role earn between $50.96 and $78.61 per hour, depending on experience, location, and employer.

What is a clinical project leader?

Clinical Project Leaders are professionals responsible for overseeing and managing clinical trials and research projects within the pharmaceutical, biotechnology, or medical device industries. They coordinate study teams, ensure regulatory compliance, manage timelines and budgets, and serve as the main point of contact between sponsors, investigators, and regulatory bodies. Their role is essential in ensuring that clinical studies are conducted efficiently, ethically, and in accordance with all protocols and regulations.

What are the key skills and qualifications needed to thrive as a clinical project leader?

To thrive as a Clinical Project Leader, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a relevant degree and experience in the pharmaceutical or clinical trials industry. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and project management certifications like PMP are highly valuable. Exceptional leadership, problem-solving, and communication skills help drive team performance and stakeholder engagement. These competencies are essential to ensure that clinical projects are completed efficiently, compliantly, and to the highest quality standards.

What are some common challenges clinical project leaders face when managing multi-site clinical trials?

Clinical Project Leaders often encounter challenges related to coordinating activities across various trial sites, ensuring regulatory compliance, and maintaining consistent communication among cross-functional teams. Overseeing timelines and budgets while adapting to unforeseen issues, such as patient recruitment delays or protocol amendments, requires strong organizational and problem-solving skills. Effective collaboration with clinical research associates, data managers, and investigators is essential for overcoming these obstacles and ensuring the trial's success.

What does a clinical project leader do?

A clinical project leader oversees the planning, execution, and management of clinical trials to ensure they are completed on time, within scope, and budget. They coordinate with cross-functional teams, monitor progress, ensure compliance with regulatory standards, and utilize project management tools to deliver high-quality results.
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Infographic showing various Clinical Project Leader job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $131,045 per year, or $63 per hour.

Clinical Project Manager

Baltimore, MD • On-site

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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