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Clinical Research Associate Manager Jobs in Raleigh, NC

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Conduct, drive, and manage country-specific feasibility and site pre-qualification and ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

IQVIA

Clinical Research Associate

Durham, NC · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... Successful candidates will possess strong site management skills, a commitment to quality, and the ...

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 ... Under management supervision, the Sr. CRA will monitor assigned clinical trials to ensure adherence ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

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 ... Job Overview Perform monitoring and site management work to ensure that sites are conducting the ...

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 ... Job Overview Perform monitoring and site management work to ensure that sites are conducting the ...

IQVIA, Inc.

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 ... Job Overview Perform monitoring and site management work to ensure that sites are conducting the ...

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Clinical Research Associate Manager information

See Raleigh, NC salary details

$35K

$84K

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How much do clinical research associate manager jobs pay per year?

As of Aug 25, 2026, the average yearly pay for clinical research associate manager in Raleigh, NC is $84,037.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $110,800.00 per year, depending on experience, location, and employer.

What is a clinical research associate manager?

A Clinical Research Associate Manager is a professional responsible for overseeing and managing a team of Clinical Research Associates (CRAs) who monitor clinical trials to ensure they are conducted according to protocols, regulatory requirements, and good clinical practice. They coordinate trial activities, provide guidance and training to CRAs, and serve as a liaison between the research team, sponsors, and regulatory bodies. Their role is crucial for maintaining the quality and integrity of clinical research studies.

What are the key skills and qualifications needed to thrive as a clinical research associate manager, and why are they important?

To thrive as a Clinical Research Associate Manager, you need expertise in clinical trial management, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and project management certifications like PMP are commonly required. Strong leadership, communication, and problem-solving skills help you effectively oversee teams and ensure adherence to protocols. These skills are crucial for ensuring high-quality research, regulatory compliance, and successful project delivery in clinical studies.

What are some common challenges faced by clinical research associate managers when overseeing multiple clinical trials simultaneously?

Clinical Research Associate Managers often face the challenge of balancing oversight across several ongoing clinical trials, each with unique protocols and site requirements. Managing competing deadlines, ensuring regulatory compliance, and maintaining clear communication across diverse teams are critical aspects of the role. Effective prioritization, strong organizational skills, and proactive risk management are essential to navigate these complexities and ensure trial success. Collaboration with CRAs, investigators, and cross-functional departments helps in addressing site issues promptly and maintaining study quality.

Is it hard to get a clinical research associate manager job?

Securing a clinical research associate manager position can be competitive, often requiring several years of experience in clinical research, strong leadership skills, and relevant certifications such as CCRP or RAC. Candidates with a background in clinical operations, good understanding of regulatory requirements, and proficiency with trial management tools tend to have better prospects.

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

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

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

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

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

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

Clinical Research Associate Manager jobs near you
Infographic showing various Clinical Research Associate Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $84,037 per year, or $40.4 per hour.

Senior Clinical Research Associate

Raleigh, NC • On-site

Parexel
Pharmaceutical and Medicine Manufacturing • 10K+ employees

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 74 rated research

Great coworkers

People enjoy working here

Good employer

Learn more about Parexelexternal

Full-time

Posted 15 days ago

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
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About PAREXEL

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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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