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Clinical Project Manager Jobs in Kentucky (NOW HIRING)

$110 - $160/hr

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 ...

$126 - $351/hr

Job Overview Clinical Project Management Directors direct and manage the team responsible for clinical delivery of complex; global full service, multi-regional studies and/or programs. Has strategic ...

New

$93 - $233/hr

IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine . As a Project Manager, you'll drive operational excellence ...

New

$60 - $110/hr

Job Summary The Clinical Project Specialist position is responsible for providing administrative and project management support for assigned clinical studies and projects, working closely with study ...

New

$93 - $233/hr

Senior Clinical Project Manager - Global Study Leadership At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic ...

$90 - $130/hr

Lotus Clinical Research Project Manager Full Time CRO Remote, US Company: Lotus Clinical Research Job Title: Clinical Research Project Manager Location: Lotus Clinical Research 100% Remote The ...

$112 - $222/hr

## Project Manager - Oncology - US/Canada - RemoteApplyremote type: Remotelocations: Virtual United ... We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ...

$129 - $255/hr

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide**Worldwide Clinical Trials Project ...

$120 - $180/hr

A Clinical Project Manager with at least 5 years of industry experience * Proven experience in outcomes adjudication and patient enrollment within the pharmaceutical or CRO industry. * Strong ...

New

$112 - $222/hr

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Manager does at Worldwide The Project Manager (PM) will manage one or more ...

$153 - $304/hr

Worldwide Clinical Trials Project management is the perfect blend of operational rigor and ... therapeutic expertise, with a client-focused approach. Our Global Project Leads (GPLs) and Clinical ...

$103 - $286/hr

We are seeking an experienced Associate Clinical Project Management Director to lead the strategic planning, execution, and delivery of complex global clinical trials while ensuring exceptional ...

New

$60 - $80/hr

You will maintain clinical trial management systems and tracking tools, actively participating in cross‑functional teams to ensure delivery of project deliverables. This position is remote based in ...

New

$110 - $150/hr

This role serves as the operational backbone of the department by leading clinical project management efforts, supporting data-driven decision‐making, and ensuring high‑quality execution of ...

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Showing results 1-20

Clinical Project Manager information

See Kentucky salary details

$25

$52

$94

How much do clinical project manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical project manager in Kentucky is $52.72, according to ZipRecruiter salary data. Most workers in this role earn between $36.73 and $61.78 per hour, depending on experience, location, and employer.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

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 expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

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

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.

What are the most commonly searched types of Clinical Project jobs in Kentucky?

The most popular types of Clinical Project jobs in Kentucky are:

What are popular job titles related to Clinical Project Manager jobs in Kentucky?

For Clinical Project Manager jobs in Kentucky, the most frequently searched job titles are:

What cities in Kentucky are hiring for Clinical Project Manager jobs?

Cities in Kentucky with the most Clinical Project Manager job openings:

Infographic showing various Clinical Project Manager job openings in Kentucky as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $109,662 per year, or $52.7 per hour.

$110 - $160/hr

Other

Medical, Dental, Vision, Life, PTO

Posted 5 days ago


Job description

At Clario, a part of Thermo Fisher Scientific, we help accelerate the development of life-changing therapies by delivering innovative endpoint data solutions that bring clarity and confidence to clinical research.

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 through closeout. If you thrive in a fast-paced, collaborative environment and enjoy building strong relationships with sponsors, sites, and internal teams.

What We Offer
  • Competitive compensation
  • Medical, dental, and vision coverage
  • Flexible and paid time off
  • Remote and hybrid work options
  • Tuition reimbursement
  • Employee assistance and wellness programs
  • Life and disability insurance
What You'll Be Doing
  • Lead study start-up activities by reviewing protocol requirements, developing project plans, defining timelines and milestones, and coordinating project documentation.
  • Establish and maintain project communication plans, reporting schedules, and stakeholder updates for sponsors and internal leadership.
  • Identify project success metrics, oversee project progress, and proactively manage risks, resources, and operational challenges.
  • Manage project finances, including forecasting, billing activities, scope reviews, amendments, revenue reporting, and pass-through costs.
  • Ensure compliance with study protocols, Standard Operating Procedures (SOPs), applicable regulations, and quality requirements.
  • Coordinate data collection activities across sites and collaborate with internal and external stakeholders to support successful project delivery.
  • Provide leadership to project teams by setting expectations, facilitating training, mentoring team members, and promoting a collaborative working environment.
  • Communicate protocol clarifications and revisions to project teams and ensure consistent understanding of study requirements.
  • Support business development activities through client presentations, capability discussions, investigator meetings, and representation at industry events.
  • Oversee project closeout activities, including submission support, final deliverables, and study completion activities.
  • Perform supervisory responsibilities as needed, including performance management, employee development, hiring support, and workforce planning.
  • Drive continuous improvement initiatives that enhance departmental processes, project outcomes, and customer satisfaction.
What We Look For
  • Bachelor's degree in Life Sciences, Pharmacy, Nursing, Healthcare, or a related field, or equivalent combination of education and experience.
  • Experience managing clinical research projects involving investigational products within a Contract Research Organization (CRO) or pharmaceutical environment.
  • Clinical trial experience and demonstrated ability to manage multiple projects, timelines, and stakeholders.
  • Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and U.S. Food and Drug Administration (FDA) regulations.
  • Experience with project planning, budgeting, forecasting, financial tracking, and resource management.
  • Proficiency with Microsoft Office applications, including Word, Excel, and Project.
  • Knowledge of medical imaging technologies or imaging-focused clinical studies is preferred.
  • Strong communication, presentation, stakeholder management, and relationship-building skills.
  • Demonstrated leadership, organizational, problem-solving, and decision-making capabilities.
  • Ability to work effectively in a collaborative, fast-paced, and results-driven environment.

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It's a cause that unites and inspires us. It's why we come to work and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Clario, a part of Thermo Fisher Scientific is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Clario Privacy Policy

Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.

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