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Pharmaceutical Research Associate Jobs in Raleigh, NC

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site +1

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Labcorp is seeking a Sr. Clinical Research Associate - Oncology Evidence Generation to join our ...

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 ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Labcorp is seeking a Sr. Clinical Research Associate - Oncology Evidence Generation to join our ...

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All JobsPharmaceutical Research Associate JobsPharmaceutical Research Associate Jobs in Raleigh, NC

Pharmaceutical Research Associate information

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$15

$31

$45

How much do pharmaceutical research associate jobs pay per hour?

As of Sep 13, 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.

Clinical Research Associate II / Senior Clinical Research Associate

Raleigh, NC • On-site, Remote

410 ICR United States USA
See more jobs at 410 ICR United States USAexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago

Job description

North America | Remote | Sponsor-Dedicated (FSP) Opportunities

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.

About the Opportunity

As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.

Depending on your experience level, you may:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure protocol compliance, patient safety, data quality, and regulatory adherence
  • Build strong relationships with investigative sites and key stakeholders
  • Identify and proactively resolve site and study issues
  • Collaborate with cross-functional teams to support successful study delivery
  • Support inspection readiness and high-quality study execution
  • Mentor and guide less experienced CRAs (Senior CRA level)

What We're Looking For

CRA II

  • Bachelor's degree in a scientific, healthcare, or related field
  • Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
  • Ability to work independently while collaborating effectively across teams

Senior CRA

  • Significant clinical monitoring experience across multiple studies and sites
  • Advanced knowledge of clinical trial processes, regulations, and site management
  • Proven ability to manage priorities and drive study quality independently
  • Experience mentoring or supporting other CRAs is advantageous

For all applicants

  • Strong communication and relationship-building skills
  • Willingness to travel as required
  • Passion for advancing clinical research and improving patient outcomes

When you join ICON Strategic Solutions, you gain the best of both worlds:

  • Work within dedicated sponsor environments
  • Build expertise with leading global pharmaceutical and biotechnology companies
  • Access diverse opportunities across multiple therapeutic areas
  • Benefit from ICON's global scale, career development, and support network
  • Join a culture focused on innovation, collaboration, and patient impact
  • Competitive compensation and benefits package

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply