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Sr Clinical Research Associate Jobs in Raleigh, NC

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

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 ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

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 ...

New

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

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 ...

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 support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

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:

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Showing results 1-20

All JobsSr Clinical Research Associate JobsSr Clinical Research Associate Jobs in Raleigh, NC

Sr Clinical Research Associate information

See Raleigh, NC salary details

$35K

$91.7K

$139.5K

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

As of Aug 14, 2026, the average yearly pay for sr clinical research associate in Raleigh, NC is $91,676.00, 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.

Is it hard to get a Sr Clinical Research Associate job?

Securing a Sr Clinical Research Associate position can be competitive, as it typically requires relevant experience in clinical trials, strong knowledge of Good Clinical Practice (GCP), and often a relevant degree or certification. Candidates with proven project management skills and familiarity with clinical trial management systems tend to have better prospects. The hiring process may involve multiple interviews and assessments of technical expertise.

What is the difference between Sr Clinical Research Associate vs Clinical Research Associate?

AspectSr Clinical Research AssociateClinical Research Associate
Required credentialsBachelor's degree, experience, often certifications like CCRP or RACBachelor's degree, entry-level or less experience, certifications optional
Work environmentPharmaceutical companies, CROs, clinical trial sitesSimilar settings, often entry-level roles in clinical trials
Employer and industry usageUsed in pharmaceutical and biotech industries, more senior rolesCommon in clinical research, entry to mid-level roles
Search and comparison intentOften searched for career progression or senior rolesOften searched for entry-level positions or understanding roles

The main difference between a Sr Clinical Research Associate and a Clinical Research Associate lies in experience, responsibilities, and qualifications. The senior role typically requires more experience, certifications, and involves overseeing complex trials, while the CRA is often an entry-level or mid-level position focused on supporting clinical trial activities.

What is a Sr Clinical Research Associate?

A Sr Clinical Research Associate (Senior CRA) is an experienced professional responsible for overseeing clinical trials to ensure they comply with regulatory requirements, protocols, and Good Clinical Practice (GCP) guidelines. They monitor study sites, review data, ensure participant safety, and act as a liaison between the sponsor and clinical sites. Senior CRAs often mentor junior staff, manage multiple studies, and contribute to improving clinical trial processes. Their role is vital in bringing new medical treatments and devices from research to market.

What are the key skills and qualifications needed to thrive as a Sr Clinical Research Associate?

To thrive as a Sr Clinical Research Associate, you need a robust background in clinical research, regulatory compliance, and study monitoring, usually supported by a bachelor's degree in life sciences and significant industry experience. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valued. Outstanding attention to detail, strong organizational skills, and effective communication enable successful oversight of trial sites and collaboration with study teams. These skills are vital for ensuring the integrity, safety, and compliance of clinical trials, directly impacting study outcomes and regulatory approval.

What does a senior clinical research associate do?

A senior clinical research associate (CRA) oversees and monitors clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They coordinate with study sites, review data quality, and may mentor junior staff, often using electronic data capture systems and maintaining detailed documentation throughout the trial process.

What are some common challenges faced by a Sr Clinical Research Associate when monitoring multiple clinical trial sites?

As a Sr Clinical Research Associate (CRA), juggling multiple trial sites can be challenging due to varying site compliance levels, differing investigator engagement, and diverse patient populations. You may encounter issues such as inconsistent data entry, protocol deviations, and varying levels of site staff training. Effective time management, strong communication skills, and a proactive approach to problem-solving are essential to ensure all sites adhere to protocols and timelines. Additionally, frequent travel and adapting to each site's workflow can add complexity, but these challenges also provide valuable opportunities for professional growth.

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

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

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

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

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

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

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

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

Sr Clinical Research Associate jobs near you
Infographic showing various Sr Clinical Research Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $91,676 per year, or $44.1 per hour.

Senior Clinical Research Associate

Parexel

Raleigh, NC • On-site

Full-time

Posted 4 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

29th 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

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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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