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Clinical Project Management Jobs (NOW HIRING)

ProPharma Group

Approximately 4-6 years of industry experience, including direct clinical project management experience What We're Looking For * A resilient, adaptable professional who remains focused and effective ...

Telix Pharmaceuticals (AMER)

OR · On-site

See Yourself at Telix The Clinical Project Manager (CPM) is responsible to support and oversee the ... Provide day-to-day study management including, but not limited to oversight of CRO, study vendors ...

Calyxo, Inc.

Clinical Project Manager

Pleasanton, CA

$140K - $150K/yr

Develop project management tools to manage clinical projects * Develop study tracking tools and metrics and report to management * Conduct and summarize literature reviews in support of clinical ...

Chipton Ross

Clinical Project Manager

Skaneateles, NY · On-site

$118.90/hr

Minimum 5 years of clinical operations experience (pharma, biotech, or medical device) * 1-2+ years ... Strong project management skills * Knowledge of arrhythmias, ECG interpretation, or ambulatory ...

ClinChoice

Senior Clinical Project Manager

OR · On-site +1

Collaborate in the overall management of the project with the assigned Biometrics team and with all ... Prepare the SOPs relating to clinical research activities in collaboration with the Quality System ...

Crinetics Pharmaceuticals

Clinical Project Manager

$119K - $149K/yr

Partner with Project and Portfolio Management to update resource demand and supply information on a regular basis. * Develop program scenario plans and support lifecycle management activities as ...

ClinChoice

Senior Clinical Project Manager

Collaborate in the overall management of the project with the assigned Biometrics team and with all ... Prepare the SOPs relating to clinical research activities in collaboration with the Quality System ...

ClinChoice

Senior Clinical Project Manager

Collaborate in the overall management of the project with the assigned Biometrics team and with all ... Prepare the SOPs relating to clinical research activities in collaboration with the Quality System ...

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How much do clinical project management jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for clinical project management 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 are the key skills and qualifications needed to thrive as a Clinical Project Manager, and why are they important?

To thrive as a Clinical Project Manager, you need a strong background in clinical research, project management, and regulatory compliance, often supported by a life sciences degree and relevant industry experience. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and project management certifications like PMP are highly valued. Outstanding organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These competencies ensure clinical trials are conducted efficiently, compliantly, and within budget, ultimately supporting successful study outcomes.

What are some of the common challenges Clinical Project Managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing timelines with various stakeholders, and handling regulatory documentation for different regions. Communication is key, as PMs must keep both internal teams and external partners aligned despite geographic and cultural differences. Effective risk management and proactive problem-solving skills are essential to keep studies on track and maintain data quality.

What is clinical project management?

Clinical project management involves planning, coordinating, and overseeing clinical trials or research projects to ensure they are completed on time, within budget, and according to regulatory requirements. Clinical project managers are responsible for managing cross-functional teams, timelines, budgets, and resources, as well as communicating with stakeholders and ensuring compliance with Good Clinical Practice (GCP) guidelines. Their work is essential to the successful execution of clinical studies and the advancement of new medical treatments.

What degree do you need to be a clinical project manager?

A clinical project manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or healthcare administration. Many employers prefer candidates with a master's degree or relevant certifications like PMP (Project Management Professional) to demonstrate project management skills and industry knowledge.

What is the highest paid project manager?

In clinical project management, the highest paid professionals are often senior or program managers with extensive experience, specialized skills, and certifications like PMP or PMI-ACP. Salaries can exceed $150,000 annually, especially in the pharmaceutical or biotech industries, and may include bonuses and other incentives based on project scope and complexity.

What is the difference between Clinical Project Management vs Clinical Research Associate?

AspectClinical Project ManagementClinical Research Associate
CredentialsTypically requires a degree in life sciences, project management certification (e.g., PMP)Usually holds a degree in life sciences or healthcare; certifications like CCRA are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates across departmentsMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageUsed by pharmaceutical, biotech companies, and CROs for overseeing projectsEmployed by sponsors, CROs, and sites to ensure trial quality and compliance

Clinical Project Managers focus on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. Clinical Research Associates primarily monitor clinical sites and ensure compliance with protocols. Both roles are essential in the clinical research process but differ in scope and responsibilities.

More about Clinical Project Management jobs
What cities are hiring for Clinical Project Management jobs? Cities with the most Clinical Project Management job openings:
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Clinical Project Management jobs near you
Infographic showing various Clinical Project Management job openings in the United States as of May 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.
Clinical Project Manager

Clinical Project Manager

ProPharma Group

On-site

Full-time

Posted yesterday

Job description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

We are seeking a Clinical Project Manager to lead and deliver clinical studies across Europe. This is an opportunity for someone who naturally takes initiative, follows through on commitments, and brings energy and determination to every stage of a project. You will play a central role in guiding studies from planning through execution, ensuring timelines, quality, and compliance standards are consistently met.

This role suits someone who thrives in a fast-paced environment, remains steady under pressure, and approaches challenges with a proactive, solutions-focused mindset.

Key Responsibilities
  • Lead the planning, execution, and delivery of clinical trials with a primary focus on EU projects
  • Translate project goals into clear, structured, and actionable plans
  • Coordinate cross-functional teams and stakeholders to ensure alignment and progress
  • Monitor study timelines, budgets, and quality metrics
  • Identify risks and implement mitigation strategies
  • Support, guide, and mentor junior team members where needed
  • Ensure all activities comply with applicable regulatory requirements and internal processes
Requirements
  • Strong ability to understand, explain, and communicate project concepts, and convert them into detailed execution plans
  • High level of attention to detail, accuracy, and organization
  • Excellent interpersonal and team collaboration skills
  • Outstanding communication and presentation skills (both written and verbal), with the ability to inform, influence, and motivate stakeholders
  • Solid knowledge of FDA and/or regional regulations, ICH GCP Guidelines, and clinical trial regulatory requirements
  • Experience working with clinical systems such as eTMF, CTMS, EDC, DCT, and related platforms
  • Experience managing projects and/or mentoring junior staff
  • Bachelor's degree or advanced degree (Master's, PharmD, PhD preferred), or equivalent combination of education and experience
  • Approximately 4-6 years of industry experience, including direct clinical project management experience
What We're Looking For
  • A resilient, adaptable professional who remains focused and effective in dynamic environments
  • Someone who brings a positive outlook and genuine enthusiasm to their work
  • A self-starter who naturally takes responsibility and drives projects forward
  • A collaborative team player who builds strong working relationships

If you're ready to take the lead on impactful clinical projects and contribute to a growing, collaborative environment, we'd love to hear from you.

#LI-LH1

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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