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Clinical Project Manager Jobs in Addison, TX (NOW HIRING)

Project Manager | $120,000 - $128,000 per year plus bonus | Direct Hire | Carrollton, TX What Matters Most: * Competitive base salary with total earning potential of approximately $156,000 - $172,000 ...

Project Manager Position Responsibilities Project Manager Location: Addison, TX, Plano, TX (Not more than 45 miles) Look for nearby Candidates (only w2) Note: Client is looking for a Project Manager ...

The PMO team can work remotely from Baton Rouge, LA, or follow a hybrid schedule in Plano, TX or Charlotte, NC. For the right candidate, this position may be remote, provided the individual resides ...

The Project Manager serves within the Project Management Office (PMO) at ACU Dallas, supporting cross-functional initiatives across departments such as Enrollment, Marketing, Student Services, IT, ...

Project Manager Overview Join our manufacturing team as a Project Manager, leading electrical panel projects from start to finish. Develop strategies, manage budgets and schedules, coordinate teams ...

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Clinical Project Manager information

See Addison, TX salary details

$28

$58

$104

How much do clinical project manager jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical project manager in Addison, TX is $58.76, according to ZipRecruiter salary data. Most workers in this role earn between $40.96 and $68.89 per hour, depending on experience, location, and employer.

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 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.

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 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 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 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 are popular job titles related to Clinical Project Manager jobs in Addison, TX? For Clinical Project Manager jobs in Addison, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Project Manager jobs in Addison, TX look for? The top searched job categories for Clinical Project Manager jobs in Addison, TX are:
What cities near Addison, TX are hiring for Clinical Project Manager jobs? Cities near Addison, TX with the most Clinical Project Manager job openings:
Infographic showing various Clinical Project Manager job openings in Addison, TX as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $122,228 per year, or $58.8 per hour.

Project Manager Clinical Research, Pediatrics

UT Southwestern Medical Center

Dallas, TX • On-site

$70K - $90K/yr

Full-time

Medical, Retirement, PTO

Posted 13 days ago


UT Southwestern rating

7.9

Company rating: 7.9 out of 10

Based on 152 frontline employees who took The Breakroom Quiz

109th of 887 rated healthcare providers


Job description

WHY UT SOUTHWESTERN?
With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career! 
JOB SUMMARY
Work under moderate supervision to initiate and manage research projects and programs within a department. 

This position will be overseeing the planning, implementation, and management of research projects for Dr. Martin's Sickle Cell program, ensuring alignment with defined scientific objectives and allocated effort, working directly with study Principal Investigators (Pl).

Project Leadership: Lead and manage complex research projects and study timelines.

Contracts & Agreements Management: Oversee research contracts, subawards, and sponsor agreements.

Study Start-Up & Regulatory Oversight: Manage IRB submissions, regulatory compliance, and multisite studies.

Project Coordination & Process Development: Develop workflows, improve processes, and coordinate stakeholders.

Data Management & Chart Abstraction: Maintain databases, ensure data quality, and support reporting and analysis.

Study Visit Coordination & Conduct: Coordinate research visits and ensure protocol compliance.

Participant Tracking & Retention: Support participant recruitment, enrollment, and long-term follow-up.

Communication: Collaborate with investigators, sponsors, regulatory offices, and external partners.

Grantsmanship & Scholarly Products: Support grant applications, manuscripts, abstracts, and presentations.
 

BENEFITS
UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

  • PPO medical plan, available day one at no cost for full-time employee-only coverage
  • 100% coverage for preventive healthcare-no copay
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer
  • Learn more about these and other UTSW employee benefits!


EXPERIENCE AND EDUCATION
Required

  • Education
    Bachelor's Degree in related field. 
     
  • Experience
    5 years experience in clinical research, including at least three years experience in project management, which may include management of specific clinical trials or clinical trials-related programs. 
     

Preferred

  • Education
    Advanced degree preferred. 
     
  • Experience
    Prior experience in the UTSW clinical research mentoring program is highly desirable, and participation in the UTSW clinical research mentoring program may count as additional experience. 
     


JOB DUTIES

  • For new research projects or programs, define project/program scope with the PI, goals and deliverables that support business goals in collaboration with the Clinical Research Manager, Clinical Department Administrator, and Vice Chair/Chair; assist PI to develop project plans, timelines, and associated communications documents; clearly and timely communicate project expectations to team members and management.
  • Estimate research resources and personnel needed to achieve project/program goals, and work with CRM to help allocate from within the department or externally.
  • Set and continually manage research project expectations with PIs and other team members; delegate tasks and responsibilities to appropriate personnel; identify and resolve issues and conflicts within the research team or program; identify and manage related issues.
  • Plan and schedule project timelines and milestones using appropriate tools; track project milestones and deliverables; develop and deliver progress reports.
  • Compose, edit, or create research personnel training documents. Align business processes with systems changes and provide a mechanism to deliver information to staff and/or faculty as necessary.
  • Develop best practices and tools for research project execution and management.
  • Work with PIs on scientific writing in grant proposal development, IRB development.
  • Coordinate execution of clinical trials following trial guidelines.
  • May supervise staff in performance of duties.
  • Performs other duties as assigned.

SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
EEO
UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.
 


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