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Clinical Project Associate Jobs in Raleigh, NC (NOW HIRING)

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to ... May work on highly visible projects in high-pressure situations * Must have working knowledge of ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC · On-site

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC · On-site

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH ... Collaborate and liaise with study team members for project execution support as appropriate. If ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH ... Collaborate and liaise with study team members for project execution support as appropriate. If ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site +1

Organize and lead project meetings, investigator calls, and cross-functional updates; document and ... Clinical Research Associate (CRA) or in a comparable clinical research role. * 3 or more years ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site

Organize and lead project meetings, investigator calls, and cross-functional updates; document and ... Clinical Research Associate (CRA) or in a comparable clinical research role. * 3 or more years ...

IQVIA

Clinical Research Associate

Durham, NC · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... Collaborate cross-functionally with project teams to support study execution and achievement of ...

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All JobsClinical Project Associate JobsClinical Project Associate Jobs in Raleigh, NC

Clinical Project Associate information

See Raleigh, NC salary details

$10

$27

$47

How much do clinical project associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical project associate in Raleigh, NC is $27.09, according to ZipRecruiter salary data. Most workers in this role earn between $18.17 and $35.72 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

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

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Raleigh, NC?

The most popular types of Clinical Project jobs in Raleigh, NC are:

What are popular job titles related to Clinical Project Associate jobs in Raleigh, NC?

For Clinical Project Associate jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Project Associate jobs in Raleigh, NC look for?

The top searched job categories for Clinical Project Associate jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Project Associate jobs?

Cities near Raleigh, NC with the most Clinical Project Associate job openings:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Raleigh, NC as of September 2026, with employment types broken down into 5% As Needed, 85% Full Time, 5% Part Time, and 5% Contract. Highlights an 73% In-person, 11% Hybrid, and 16% Remote job distribution, with an average salary of $56,340 per year, or $27.1 per hour.

Associate Clinical Safety Surveillance Director

Chapel Hill, NC • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 14 days ago

Job description

Associate Clinical Safety Surveillance DirectorResponsibilities
  • Oversee management of SAEs and events of special interest across UT sponsored clinical trials; provide strategic direction to team and vendors to improve efficiency, quality, and compliance.
  • Support safety governance, inspection readiness, and sustained regulatory compliance for the UT Sponsored Clinical Trial portfolio.
  • Evaluate and execute process changes in response to regulatory updates for end-to-end SAE and AESI handling.
  • Maintain and monitor unified SAE/AESI handling operating procedures (e.g., Safety Management Plan); ensure processing/submission per UT SOPs and industry standards.
  • Provide strategic guidance for developmental PV case management and reporting of ICSSRs.
  • Serve as main point of contact for day-to-day questions and issue escalation on SAE/AESI handling; manage GPS clinical trial oversight team metrics.
  • Develop and deliver training/materials for SAE/AESI handling; lead direct reports (training, performance, coaching/mentoring, career development, recruitment support as needed).
  • Lead inspection/audit readiness; perform root cause analysis and ensure CAPA; review/approve deviations/CAPAs.
  • Develop and implement new/revised SOPs; update procedural documents for SAE/AESI case handling.
  • Stay current on global/local GCP and GVP regulations supporting clinical trials in PV.
Minimum Requirements
  • BS in related field or BSN with 12+ years, or MS with 10+ years, or PharmD/PhD/MD/DO (or international equivalent) with 7+ years in pharmacovigilance end-to-end ICSR case processing.
  • 5+ years vendor management and/or CT oversight; 5+ years clinical trial or product development.
  • 3+ years people management.
  • Argus experience (preferred) and/or other safety databases.
  • End-to-end case processing (data entry, QC, medical review, regulatory submissions).
  • Project management; drug development and registration safety knowledge; global regulations/guidelines; MedDRA coding; strong written/verbal and analytical skills; cross-functional effectiveness; ability to challenge current state; adaptable in ambiguity.
  • Prior clinical PV management experience.
Job Location/Work Schedule
  • Durham, NC office with hybrid schedule (at least 3 days in office each week).
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