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Cro Clinical Project Coordinator Jobs (NOW HIRING)

Clario

... and coordinating project documentation. * Establish and maintain project communication plans ... Research Organization (CRO) or pharmaceutical environment. * Clinical trial experience and ...

Terumo Corporation

Clinical Project Manager

Somerset, NJ · On-site

... coordination of clinical data management, data analysis functions, and CRO and Vendor selection and management. Job Details/Responsibilities * Support the development of project related deliverables ...

Medical Affairs

Clinical Project Manager

Somerset, NJ

... coordination of clinical data management, data analysis functions, and CRO and Vendor selection and management. Job Details/Responsibilities * Support the development of project related deliverables ...

Terumo Corporation

Clinical Project Manager

Somerset, NJ · On-site

... coordination of clinical data management, data analysis functions, and CRO and Vendor selection and management. Job Details/Responsibilities * Support the development of project related deliverables ...

Laborie

Clinical Project Manager

Minnetonka, MN

$130K - $135K/yr

Minimum 2 years of clinical project management experience at a sponsor or CRO company is preferred. * Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN. * ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project ManagerSalary Range: $80K-$135KLocation: Baltimore, MD Unfortunately, we cannot ... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ...

Pharmaron

Clinical Project Manager

Baltimore, MD

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ...

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Cro Clinical Project Coordinator information

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$44K

$74.9K

$105.5K

How much do cro clinical project coordinator jobs pay per year?

As of Sep 14, 2026, the average yearly pay for cro clinical project coordinator in the United States is $74,949.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $94,000.00 per year, depending on experience, location, and employer.

What is a CRO clinical project coordinator?

CRO Clinical Project Coordinators are professionals who oversee and manage various aspects of clinical trials for Contract Research Organizations (CROs). They support project managers by coordinating study activities, maintaining documentation, ensuring compliance with regulatory requirements, and facilitating communication among study sites and sponsors. Their role is essential in ensuring that clinical trials run smoothly, on schedule, and within budget. They are key players in the success of pharmaceutical and medical research projects.

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

To thrive as a CRO Clinical Project Coordinator, you need knowledge of clinical trial processes, regulatory requirements, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Excellent organizational skills, attention to detail, and effective communication set top performers apart in this role. These skills are critical for ensuring clinical trials run smoothly, stay compliant, and meet project timelines in a highly regulated environment.

What are some common challenges faced by a CRO clinical project coordinator and how can they be managed effectively?

CRO Clinical Project Coordinators often encounter challenges such as balancing multiple studies simultaneously, managing tight timelines, and ensuring consistent communication between sponsors, sites, and internal teams. To manage these challenges effectively, it’s important to develop strong organizational skills, utilize project management tools, and establish clear communication channels. Proactively identifying potential bottlenecks and addressing them early can help ensure projects stay on track and compliance with regulatory standards is maintained.

What is the difference between Cro Clinical Project Coordinator vs Clinical Research Associate?

AspectCro Clinical Project CoordinatorClinical Research Associate
CredentialsBachelor's degree in life sciences or related field; certifications like CAPM or PMP are commonBachelor's degree in life sciences; often holds CRA certification
Work EnvironmentManages clinical trial projects, coordinates teams, and oversees study timelinesMonitors clinical sites, ensures protocol compliance, and verifies data accuracy
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical trial sites

The Cro Clinical Project Coordinator focuses on managing overall project timelines and team coordination, while the Clinical Research Associate primarily monitors clinical sites and ensures compliance. Both roles require similar educational backgrounds and certifications, often working within the same industry environments.

What are popular job titles related to Cro Clinical Project Coordinator jobs?

For Cro Clinical Project Coordinator jobs, the most frequently searched job titles are:

Infographic showing various Cro Clinical Project Coordinator 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 $74,949 per year, or $36 per hour.

Clinical Project Manager

Minnetonka, MN • On-site

Laborie Medical Technologies Corp
Retail • 501 - 1,000 employees
Learn more about Laborie Medical Technologies Corpexternal

$130K - $135K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

We believe that great healthcare is an essential safeguard of human dignity.
At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.
 
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.
 
Who We’re Looking For:
As a key member of the Clinical team, the Clinical Project Manager (CPM) is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). The CPM, in concert with the Clinical Program Manager, is accountable for achieving successful delivery of Laborie Clinical Team activities at the project level by meeting company and regulatory requirements according to time, quality/scope, and budget constraints.  
 
About the Role:
  • Proactively manage project level operational aspects of Clinical Research Team (CRT) including management of trial timeline, budget, resources, and vendors.
  • Provide efficient updates on trial progress to the Clinical Program Manager and/or Chief Technology Officer, with respect to vendor selection, project plans, trial budget and timeline management, quality standards and risk mitigation.
  • Lead sponsor study startup process, including but not limited to conduct of the Trial Kick-off meeting, the setup of trial master file (TMF), site selection and finalization of site and vendor Clinical Trial Agreements and budgets.
  • Ensure effective project plans are in place and operational for each trial and work proactively with the Clinical Research Team to set priorities in accordance with applicable project plans, company standard operational procedures (SOPs), ICH/GCP guidelines and regulatory requirements.
  • Chair Clinical Research Team working group and vendor status update meetings and ensure meeting minutes are completed, distributed to team members, and filed in the Trial Master File (TMF) in a timely manner.
  • Monitor the quality of vendor deliverables, address quality issues with the appropriate team member and identify opportunities to improve training, execution, and quality control across the clinical team.
  • Review and approve vendor invoices in collaboration with the accounting team to ensure investigator payments occur in a timely manner.
  • Ensure all project level study documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provide oversight to the clinical team regarding TMF filing, maintenance and archival procedures 
  • Effectively provide support to the Clinical Research Team in the conduct of the trial(s). 
Minimum Qualifications:
  • Bachelor's degree in Life Sciences; Master's or Doctoral degree preferred.
  • 8+ years of clinical operations experience for CPM; with increasing levels of responsibility in the medical device or CRO industry is required.
  • Minimum 2 years of clinical project management experience at a sponsor or CRO company is preferred.
  • Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN.
  • Experience with medical devices CER, PMS, PMCF, PSUR medical writing.
  • Speak fluent English, excellent verbal and written communication skills, Microsoft Office, Excel, PowerPoint, Outlook, Teams, etc.
  • Must have thorough knowledge of clinical research concepts, practices, and FDA/EU regulations and ICH Guidelines, ISO 14155, clinical research, and data management methods.  
Why Laborie:
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
  • Paid time off and paid volunteer time
  • Medical, Dental, Vision and Flexible Spending Account
  • Health Savings Account with Company Funded Contributions
  • 401k Retirement Plan with Company Match
  • Parental Leave and Adoption Services
  • Health and Wellness Programs and Events
  • Awarded 2025 Cigna Healthy Workforce Designation Gold Level
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.
 

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