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Pharmaceutical Research Associate Jobs in Raleigh, NC

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry ... 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 ... Minimum of 2 years of independent on-site monitoring experience within the pharmaceutical ...

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Pharmaceutical Research Associate information

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$15

$31

$45

How much do pharmaceutical research associate jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for pharmaceutical research associate in Raleigh, NC is $31.63, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $35.96 per hour, depending on experience, location, and employer.

What does a pharmaceutical research associate do?

A Pharmaceutical Research Associate is responsible for supporting clinical trials and research studies that help develop new medications and treatments. Their duties include collecting and analyzing data, ensuring compliance with regulatory standards, and assisting with the documentation and reporting of research findings. They work closely with scientists, clinical investigators, and regulatory bodies to ensure the accuracy and integrity of research processes. This role is crucial in advancing medical knowledge and bringing new drugs to market safely and efficiently.

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

Pharmaceutical Research Associates often juggle several clinical trials at once, which can present challenges such as coordinating timelines, ensuring regulatory compliance, and maintaining clear communication with cross-functional teams. Balancing the priorities of different studies, troubleshooting unforeseen issues, and adapting to evolving protocols require strong organizational and problem-solving skills. Effective time management and proactive collaboration with clinical monitors, data managers, and regulatory specialists are essential to successfully navigate these complexities and maintain high-quality research standards.

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

To thrive as a Pharmaceutical Research Associate, you need a solid background in life sciences, chemistry, or pharmacology, often supported by a bachelor's or master's degree in a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) guidelines, and analytical instruments like HPLC or mass spectrometry is typically required. Strong attention to detail, critical thinking, and effective teamwork are essential soft skills for success in this role. These competencies ensure accurate data collection, regulatory compliance, and the efficient advancement of pharmaceutical research projects.

What is the difference between Pharmaceutical Research Associate vs Clinical Research Coordinator?

AspectPharmaceutical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree in life sciences, often with industry certificationsBachelor's degree in health sciences or related field, often with clinical research certifications
Work EnvironmentPharmaceutical companies, research labs, biotech firmsHospitals, clinics, research sites
Industry UsageDrug development, preclinical and clinical trials in pharmaOverseeing clinical trial processes at research sites
Job FocusAssisting in drug research, data collection, and analysisManaging patient recruitment, data entry, and trial coordination

The Pharmaceutical Research Associate primarily focuses on supporting drug development within pharmaceutical companies, while the Clinical Research Coordinator manages clinical trial activities at research sites. Both roles require similar educational backgrounds and certifications but differ in work environment and specific responsibilities.

How do I become a pharmaceutical research associate?

To become a pharmaceutical research associate, typically a bachelor's degree in pharmacy, biology, chemistry, or a related field is required. Gaining experience through internships or entry-level positions and developing skills in laboratory techniques and data analysis are important steps; some roles may also require knowledge of Good Laboratory Practices (GLP) and regulatory guidelines.

What is the role of pharmaceutical research associate in pharma?

A pharmaceutical research associate conducts experiments and analyzes data to support drug development and testing. They often work in laboratories, using scientific methods, and may assist in regulatory documentation and quality control processes.

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

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

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

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

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

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

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

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

Pharmaceutical Research Associate jobs near you
Infographic showing various Pharmaceutical Research Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $65,792 per year, or $31.6 per hour.

Senior Clinical Research Associate

Parexel

Raleigh, NC • On-site

Full-time

Posted 10 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

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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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