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Full Time Clinical Research Associate Jobs in Raleigh, NC

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

IQVIA

Clinical Research Associate

Durham, NC

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

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Senior Clinical Research Associate

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

Icon plc

Senior Clinical Research Associate

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

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/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

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All JobsClinical Research Associate JobsFull Time Clinical Research Associate JobsFull Time Clinical Research Associate Jobs in Raleigh, NC

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 Aug 16, 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 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 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 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 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $91,681 per year, or $44.1 per hour.

Senior Clinical Research Associate

Parexel

Raleigh, NC • On-site

Full-time

Posted 6 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 73 rated research

Job description

Name of Employer: Parexel International LLC
Position Title: Sr. Clinical Research Associate
*Multiple Openings Available*
Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609
*100% Remote reporting to Raleigh, NC.
Hours: Full Time / 40 hours per week
Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported data. Represent the company at assigned clinical trial sites and be accountable for quality and delivery from site identification to the close of trial. Conduct, drive, and manage country-specific feasibility and site pre-qualification and qualification activities, which include preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments. Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring, Termination Visits, and Site Motivational Visits, and generate site visit reports. Develop strategy to configure, distribute, and collect, review, and approve high-quality country-specific and site-specific documents, essential regulatory documents, and updated or amended regulatory documentation. Customize, review, and negotiate country/site-specific Informed Consent Forms, translations, and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA applications, resolve conflicts, and determine appropriate follow-up until receipt of final approval. Address and resolve issues at clinical trial sites, including the need for additional training, potential deficiencies in documentation, and communication. Follow-up on Case Report Form data entry, query status, and Serious Adverse Events. Assess and manage test article/study supply including supply, accountability, and destruction/return status. Review and follow-up on site payment status and ensure site receives payments on a timely manner. Communicate study issues that require immediate action with a proposed strategy for resolution. Ensure assigned sites are audit-ready and inspection-ready. Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring visits. Perform report review of visit reports of junior CRAs to ensure compliance with GCP and Protocol Guidelines. Guide Administrative Support Team members, review work, and provide feedback to the manager regarding performance.
Education requirements: Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 3 years of experience in clinical research.
Or, alternatively:
Education requirements : Master's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 1 year of experience in clinical research.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site Management and application of clinical trial methodology and terminology; Independently monitoring visits (Qualification, Site Initiation, and Monitoring); Working with clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines; and Communicating results to stakeholders in non-technical language.
Travel requirements: Up to 75% Domestic Travel.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #ES2401 to openings@parexel.com

What Parexel employees say

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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