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Clinical Operations Coordinator Jobs in Raleigh, NC

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

The Clinical Project Coordinator position is responsible for supporting management efforts of ... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

The Clinical Project Coordinator position is responsible for supporting management efforts of ... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ...

Parexel

Global Clinical Lead / Global Lead

Raleigh, NC · On-site

... Operations Leader * Experience leading complex global or multi-region studies * Strong knowledge of ICH GCP regulatory requirements and clinical trial processes * Experience coordinating cross ...

Parexel

Global Clinical Lead / Global Lead

Raleigh, NC · On-site

... Operations Leader * Experience leading complex global or multi-region studies * Strong knowledge of ICH GCP regulatory requirements and clinical trial processes * Experience coordinating cross ...

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Clinical Operations Coordinator information

See Raleigh, NC salary details

$13

$24

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How much do clinical operations coordinator jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for clinical operations coordinator in Raleigh, NC is $24.07, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $27.12 per hour, depending on experience, location, and employer.

What is the difference between Clinical Operations Coordinator vs Clinical Research Associate?

AspectClinical Operations CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CRA certification are common
Work EnvironmentWorks within clinical trial teams, coordinating study logistics and site managementMonitors clinical trial sites, ensuring protocol compliance and data integrity
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and healthcare institutionsCommonly employed by CROs, pharmaceutical companies, and research institutions

The Clinical Operations Coordinator and Clinical Research Associate roles share similar educational backgrounds and industry settings. However, the Coordinator focuses on coordinating trial logistics and site management, while the CRA primarily monitors trial sites and ensures compliance. Both roles are essential in clinical research but serve different functions within the trial process.

What is a clinical operations coordinator?

Clinical Operations Coordinators are professionals who manage the day-to-day administrative and operational activities within clinical settings, such as hospitals, clinics, or research organizations. They ensure that clinical trials or patient care programs run smoothly by coordinating schedules, managing documentation, and facilitating communication between healthcare teams. Their responsibilities may include regulatory compliance, budget management, and supporting patient enrollment. By streamlining these processes, Clinical Operations Coordinators play a crucial role in maintaining the efficiency and quality of clinical operations.

How does a clinical operations coordinator collaborate with clinical staff and other departments to ensure smooth trial operations?

A Clinical Operations Coordinator plays a central role in facilitating communication and coordination between clinical staff, such as nurses and physicians, and other departments like regulatory affairs, data management, and finance. They often organize meetings, distribute study updates, and address logistical challenges to keep clinical trials on track. Effective collaboration ensures that patient recruitment, data collection, and compliance requirements are met efficiently. Building strong working relationships across departments is key to resolving issues quickly and maintaining high-quality standards throughout the study lifecycle.

What are the key skills and qualifications needed to thrive as a clinical operations coordinator, and why are they important?

To thrive as a Clinical Operations Coordinator, you need strong organizational abilities, knowledge of clinical trial processes, and a relevant degree in healthcare or life sciences. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and often certifications like CCRC or SOCRA are typically required. Exceptional communication, attention to detail, and problem-solving skills help you excel in managing multiple tasks and stakeholders. These competencies are vital for ensuring smooth clinical operations, regulatory adherence, and the successful execution of clinical studies.
What are the most commonly searched types of Clinical Operations jobs in Raleigh, NC? The most popular types of Clinical Operations jobs in Raleigh, NC are:
What are popular job titles related to Clinical Operations Coordinator jobs in Raleigh, NC? For Clinical Operations Coordinator jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Operations Coordinator jobs in Raleigh, NC look for? The top searched job categories for Clinical Operations Coordinator jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Operations Coordinator jobs? Cities near Raleigh, NC with the most Clinical Operations Coordinator job openings:
Clinical Operations Coordinator jobs near you
Infographic showing various Clinical Operations Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $50,073 per year, or $24.1 per hour.

Clinical Operations Administrative Support

PSI CRO

Durham, NC • On-site

Full-time

Posted 12 days ago

Job description

Company Description

We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

Join our Clinical Operations team and help support the successful delivery of global clinical trials. As a Clinical Operations Administrative Support (COAS) you will provide administrative and operational support to clinical trial project teams, helping ensure studies are conducted efficiently, documentation is maintained accurately, and clinical sites receive the support they need throughout the trial lifecycle. This is an excellent opportunity for someone looking to build a career in clinical research.

  • Exchanges project-specific information and documents with other PSI departments, sites and vendors
  • Maintains information in study-specific and corporate tracking systems
  • Supports regulatory and ethics committee submissions and notifications
  • Assists with organization of internal team meetings
  • Under supervision, coordinates sites payments within the project team
  • Under supervision, prepares draft agendas for, and minutes of, internal team meetings
  • Under supervision, assists with preparation, conduct and follow-up of Investigator Meetings
  • Assists with clinical supplies order, receipt, inventory storage, distribution, return/recall and reconciliation at either PSI warehouse or as defined by the project team
  • Assists with preparation for and follow-up on TMF and systems audits and inspections
  • Under supervision maintains, performs regular periodic checks of, and files study related documents in the TMF on a site and country level
  • Under supervision prepares, distributes, and updates Investigator Site Files (ISF) and ISF checklists
  • Assists with translations of study-specific documents
  • Under supervision, assists with safety information flow with investigative sites
  • Other departmental assignments, as necessary
Qualifications
  • College or university science degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient.
    • Equivalency is defined as a minimum of 1 year experience in corporate or academic environment where administrative experience and technical skills have been gained.
  • Strong organizational skills with exceptional attention to detail.
  • Ability to manage multiple priorities and work effectively in a fast-paced environment.
  • Excellent written and verbal communication skills.
  • Proficiency with Microsoft Office applications.
Additional Information

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future

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