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

Allucent

Clinical Trial Leader

Cary, NC · On-site +1

... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... Liaising closely with the Project Manager (PM) and other department leaders if /whennecessary,on ...

Allucent

Clinical Trial Leader

Cary, NC · On-site +1

... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... Liaising closely with the Project Manager (PM) and other department leaders if /when necessary, on ...

Fortrea

Ophthalmology & Gen Meds - CRA II

Durham, NC · On-site

$105/hr

Coordinate designated clinical projects as a Local Project Coordinator (with supervision, ifapplicable) and may act as a local client contact as assigned * Perform other duties as assigned by ...

Allucent

Clinical Trial Leader

Cary, NC · Remote

... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... Liaising closely with the Project Manager (PM) and other department leaders if /when necessary ...

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Clinical Project Associate information

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$12

$30

$53

How much do clinical project associate jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for clinical project associate in Raleigh, NC is $30.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $40.43 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 in supporting clinical trial operations?

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, and why are they important?

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 July 2026, with employment types broken down into 7% As Needed, 86% Full Time, and 7% Contract. Highlights an 100% In-person job distribution, with an average salary of $63,768 per year, or $30.7 per hour.
Associate Director, eCOA Project Management

Associate Director, eCOA Project Management

IQVIA

Durham, NC • Remote

$100K - $278K/yr

Full-time

Posted 19 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

53rd of 207 rated it services

Job description

Join a high-growth team at the forefront of eCOA delivery, where you'll lead complex, global clinical programs that directly impact patient-centric research. As an Associate Director, you'll take on a highly visible leadership role-driving project excellence, mentoring teams, and shaping operational strategy in a dynamic and evolving environment.

Job Overview

The Associate Director, eCOA Project Management is responsible for leading complex eCOA programs, ensuring successful delivery across scope, timeline, and quality expectations. This role combines hands-on project leadership, people management, and process improvement, with accountability for both project execution and team performance.

You will oversee project managers, support escalations, contribute to account leadership activities, and drive operational excellence across the portfolio. The role is remote with occasional travel and a preference for Eastern Time Zone alignment.

Key Responsibilities

  • Define and validate project/program scope, timelines, and success metrics for complex eCOA implementations
  • Lead end-to-end project delivery, including scope, schedule, cost, and quality management
  • Identify risks and develop mitigation strategies; track and report portfolio performance
  • Manage and mentor a team of project managers (approximately 7-8 direct reports)
  • Conduct regular one-on-ones, manage performance, and support career development of team members
  • Act as first point of escalation for project and team-related issues
  • Support account leadership and client deliverables as needed
  • Partner with stakeholders to ensure alignment on project goals and outcomes
  • Lead or contribute to process improvement initiatives and SOP development
  • Drive change management, including training coordination and onboarding of new team members
  • Deliver presentations and communicate project updates to leadership and cross-functional teams

Qualifications

  • Bachelor's degree in Computer Science, Life Sciences, or a related field (or equivalent experience)
  • Approximately 5+ years of direct people management experience preferred
  • Strong project management experience in clinical technology or eCOA (preferred but not required if project management expertise is strong)
  • Demonstrated experience managing complex programs and cross-functional teams
  • Excellent communication and presentation skills (including PowerPoint, Teams, and stakeholder engagement)
  • Ability to manage multiple priorities in a fast-paced, evolving environment

Nice to Have

  • eCOA systems experience
  • Familiarity with IRT or eConsent platforms

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $100,200.00 - $278,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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