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Full Time Clinical Research Associate Jobs in Raleigh, NC

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

This full-time onsite Clinical Research Professional (CRP) will participate in research conducted ... Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant ...

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Full Time Clinical Research Associate information

See Raleigh, NC salary details

$35K

$91.7K

$139.5K

How much do full time clinical research associate jobs pay per year?

As of Sep 6, 2026, the average yearly pay for full time clinical research associate in Raleigh, NC is $91,681.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,800.00 and $124,400.00 per year, depending on experience, location, and employer.

What is a full time clinical research associate?

A Full Time Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials and ensuring that research studies comply with regulatory requirements and study protocols. CRAs play a critical role in the development of new drugs and medical devices by overseeing the progress of clinical trials, verifying data accuracy, and ensuring patient safety. They often travel to various clinical sites to conduct site visits, train staff, and review study documentation. Working full time, a CRA may handle multiple studies simultaneously and collaborate closely with investigators, sponsors, and regulatory agencies.

What are the key skills and qualifications needed to thrive as a full time clinical research associate?

To thrive as a Full Time Clinical Research Associate, you need a solid background in life sciences or a related field, familiarity with Good Clinical Practice (GCP) guidelines, and a bachelor's degree (often required). Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and understanding of regulatory requirements is crucial, and certifications like ACRP or SOCRA are often valued. Strong attention to detail, communication, and organizational skills help you effectively monitor trials and collaborate with study sites. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, which is vital for patient safety and reliable research outcomes.

What are some common challenges faced by full time clinical research associates when managing multiple clinical trials simultaneously?

Full Time Clinical Research Associates (CRAs) often juggle several studies at once, which can make prioritizing tasks and managing time effectively a challenge. Staying compliant with regulatory requirements while ensuring data accuracy and maintaining clear communication with site staff requires strong organizational skills. Additionally, frequent travel and adapting to different site environments can be demanding. CRAs who develop robust planning strategies and effective communication habits tend to navigate these challenges successfully, ensuring studies run smoothly and efficiently.

What is the difference between Full Time Clinical Research Associate vs Clinical Research Coordinator?

AspectFull Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often with clinical or life sciences background; certifications like CCRP or ACRP are commonBachelor's degree in health sciences or related field; certifications like CCRP or ACRP are also common
Work EnvironmentMonitor clinical trials at multiple sites, often traveling; work closely with sponsors and CROsManage daily trial activities at a single site; coordinate with investigators and staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites, academic institutions

While both roles require similar educational backgrounds and certifications, a Full Time Clinical Research Associate primarily monitors multiple trial sites and ensures compliance, often traveling. In contrast, a Clinical Research Coordinator manages trial activities at a single site, focusing on patient recruitment and data collection. Both roles are essential in clinical research but differ in scope and daily responsibilities.

What are popular job titles related to Full Time Clinical Research Associate jobs in Raleigh, NC?

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

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

The top searched job categories for Full Time Clinical Research Associate jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Full Time Clinical Research Associate jobs?

Cities near Raleigh, NC with the most Full Time Clinical Research Associate job openings:

Full Time Clinical Research Associate jobs near you
Infographic showing various Full Time Clinical Research Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 25% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $91,681 per year, or $44.1 per hour.

Clinical Research Associate, Sponsor Dedicated, Oncology

IQVIA

Durham, NC • On-site

$90K - $197K/yr

Full-time

Posted 9 days ago

Key responsibilities

  • Conduct site visits including selection, initiation, monitoring, and close-out to ensure compliance with GCP and ICH guidelines.

  • Collaborate with sites to develop, track, and ensure achievement of recruitment plans and study progress.

  • Provide protocol training, maintain communication with sites, and evaluate site practices for protocol adherence.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

Role Overview:As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.

Key Responsibilities:

  • Site Visits:Conduct selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Recruitment Drive:Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.
  • Training & Communication:Provide protocol training and maintain regular communication with sites to manage expectations and address issues.
  • Quality Assurance:Evaluate site practices for protocol adherence and escalate quality issues as needed.
  • Study Progress:Track regulatory submissions, recruitment, enrollment, and data management to ensure smooth study progress.
  • Documentation:Maintain essential documents in the Trial Master File (TMF) and Investigator's Site File (ISF) as per regulatory requirements.
  • Mentorship:Mentor clinical staff through co-monitoring and training visits.
  • Collaboration:Work closely with study team members to support project execution.
  • Financial Management:Manage site finances and retrieve invoices as per local requirements.

Qualifications:

  • Education:BS Degree in a scientific discipline or healthcare preferred.
  • Experience:Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.
  • Knowledge:Strong understanding of GCP and ICH guidelines, with expertise in oncology protocols.
  • Skills:Proficiency in Microsoft Office, excellent communication skills, and strong organizational and problem-solving abilities.
  • Attributes:Effective time and financial management, and the ability to build strong working relationships.

Why Join Us?Be part of a team that's driving innovation in clinical research. Your contributions will help shape the future of healthcare. Apply now and embark on a rewarding career journey with us!

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 $90,200.00 - $197,500.00. 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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