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Cra Pharmaceutical Jobs in Raleigh, NC (NOW HIRING)

410 ICR United States USA

Lead CRA

Raleigh, NC · On-site

Lead CRA ICON is a global healthcare intelligence and clinical research organisation united by a ... Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO ...

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 ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Organize shipments to CRA/Site. Includes set-up and maintenance of Index with Comments ... with pharmaceutical, biotechnology, and medical device firms. For more information, visit www ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Organize shipments to CRA/Site. Includes set-up and maintenance of Index with Comments ... with pharmaceutical, biotechnology, and medical device firms. For more information, visit www ...

RXinsider LTD.

Senior Clinical Project Manager

Raleigh, NC · On-site

$140 - $200/hr

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on ... Responsible for monthly Protocol Deviation (PD) review, including oversight of CRA documentation ...

New

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 ...

Fujifilm

CMMS Admin 1

Holly Springs, NC · On-site

$27K - $32K/yr

... CRA) and System Impact Assessments (SIA) Assists in the execution of system upgrades (e.g., user ... pharmaceuticals or biotechnology Experience with equipment maintenance and calibration processes ...

Fujifilm

CMMS Admin 1

Holly Springs, NC

$27K - $32K/yr

... CRA) and System Impact Assessments (SIA) • Assists in the execution of system upgrades (e.g ... pharmaceuticals or biotechnology • Experience with equipment maintenance and calibration ...

Fujifilm

CMMS Admin 1

Holly Springs, NC · On-site

$15.50 - $21.50/hr

... CRA) and System Impact Assessments (SIA) • Assists in the execution of system upgrades (e.g ... pharmaceuticals or biotechnology • Experience with equipment maintenance and calibration ...

Sitero LLC

Director, Business Development

Raleigh, NC · On-site

$150K - $175K/yr

Minimum of 5 years working for a Contract Research Organization (CRO), Life Sciences technology company or Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ...

Sitero LLC

Director, Business Development

Raleigh, NC

$150K - $175K/yr

Minimum of 5 years working for a Contract Research Organization (CRO), Life Sciences technology company or Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ...

Sitero LLC

Director, Business Development

Raleigh, NC · Remote

$150K - $175K/yr

Minimum of 5 years working for a Contract Research Organization (CRO), Life Sciences technology company or Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ...

All JobsCra Pharmaceutical JobsCra Pharmaceutical Jobs in Raleigh, NC

Cra Pharmaceutical information

See Raleigh, NC salary details

$10.7K

$77.2K

$133.7K

How much do cra pharmaceutical jobs pay per year?

As of Aug 21, 2026, the average yearly pay for cra pharmaceutical in Raleigh, NC is $77,214.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,100.00 and $132,700.00 per year, depending on experience, location, and employer.

What is a CRA pharmaceutical?

A Clinical Research Associate (CRA) in the pharmaceutical industry monitors clinical trials to ensure compliance with regulations, protocols, and ethical standards. They work with investigators, sponsors, and regulatory agencies to ensure accurate data collection and patient safety. CRAs may travel to trial sites, review documentation, and provide training on study procedures. Their role is critical in bringing new drugs and treatments to market efficiently and safely.

What does a CRA pharmaceutical do?

A Clinical Research Associate (CRA) in the pharmaceutical sector typically monitors clinical trials to ensure compliance with protocols and regulatory requirements, reviews data quality, and visits research sites to train staff and verify proper documentation. Daily tasks often include preparing visit reports, resolving site issues, and communicating with site coordinators and project managers. The role also involves tracking patient enrollment, ensuring the safety and rights of trial participants, and facilitating clear communication between clinical teams. As a CRA, you can expect a dynamic mix of fieldwork and remote communication, with opportunities to build strong professional relationships across the research landscape.

What are the key skills and qualifications needed for a CRA pharmaceutical?

To thrive as a Clinical Research Associate (CRA) in the pharmaceutical industry, you need a solid background in life sciences, clinical research methodologies, and Good Clinical Practice (GCP) guidelines, often supported by a relevant degree. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) software, and GCP certification are commonly required technical qualifications. Excellent organizational skills, attention to detail, and strong interpersonal communication help distinguish top performers in this field. These skills ensure trials are conducted safely, ethically, and in compliance with strict regulatory standards while facilitating effective collaboration between sites and sponsors.

How hard is it to get a CRA pharmaceutical job?

Securing a CRA (Clinical Research Associate) pharmaceutical job typically requires relevant education, such as a degree in life sciences or healthcare, and experience in clinical trials or related fields. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve chances, but competition can be high depending on the location and company requirements.

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

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

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

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

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

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

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

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

Cra Pharmaceutical jobs near you
Infographic showing various Cra Pharmaceutical job openings in Raleigh, NC as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $77,214 per year, or $37.1 per hour.

Lead CRA

410 ICR United States USA

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 29 days ago

Job description

Lead CRA

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.


We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards. You will be a key contributor to the success of clinical trials by driving site performance, providing mentorship to CRAs, and ensuring the highest levels of data quality and patient safety.

What You Will Be Doing:

  • Leading site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines.

  • Serving as the primary point of contact for clinical sites, addressing site queries, and resolving issues to maintain site engagement and performance.

  • Ensuring the integrity of clinical data by conducting thorough source data verification, reviewing site records, and monitoring for protocol deviations.

  • Mentoring and providing guidance to CRAs, contributing to their professional development and supporting the consistent application of best practices across studies.

  • Collaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials.

Your Profile:

  • Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Advanced degree preferred.

  • Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO industry, with a proven track record of managing complex clinical trials.

  • In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.

  • Strong leadership and mentoring skills, with the ability to manage and motivate CRAs and site staff effectively.

  • Excellent communication, organizational, and problem-solving skills, with a proactive approach to managing site performance and resolving issues.

  • Experience in Gene Therapy or Ophthalmology studies (complex indications)


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