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Regional Clinical Research Associate Jobs (NOW HIRING)

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - East Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Clinical Research Associate

Long Beach, CA · On-site +1

$91K - $114K/yr

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Senior Clinical Research Associate As Clinical Research Associate you will be responsible for monitoring clinical trials and ensuring investigators are conducting the research within requirements of ...

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Clinical Research Associate

Blue Bell, PA · On-site +1

$91K - $114K/yr

Clinical Research Associate - Central ICON is a global healthcare intelligence and clinical ... Our FSP program is looking for an Oncology monitor to support the Central, US region. What You Will ...

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Clinical Research Associate - Early Development Multi-Therapeutic - Regional (major hub) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new ...

Showing results 41-60

Regional Clinical Research Associate information

See salary details

$11K

$79.4K

$137.5K

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

As of Aug 8, 2026, the average yearly pay for regional clinical research associate in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are some common challenges regional clinical research associates face when managing multiple study sites?

Regional Clinical Research Associates (CRAs) often juggle overseeing several clinical trial sites, which can present challenges such as coordinating travel schedules, maintaining consistent communication with site staff, and ensuring all sites comply with study protocols and regulatory requirements. Balancing administrative duties with on-site monitoring visits requires strong organizational and time-management skills. Additionally, adapting to varying site cultures and addressing site-specific issues are essential for maintaining study quality and fostering effective collaboration.

What are the key skills and qualifications needed to thrive as a regional clinical research associate?

To thrive as a Regional Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory requirements, and a relevant life sciences degree, often complemented by industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Strong organizational, problem-solving, and communication skills help manage multiple sites, build rapport with investigators, and ensure protocol compliance. These competencies are critical for maintaining data integrity, ensuring regulatory compliance, and supporting successful clinical trial outcomes across diverse locations.

What is a regional clinical research associate?

A Regional Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials at sites within a specific geographic region. They ensure that clinical studies are conducted according to protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Regional CRAs act as a liaison between the clinical trial sponsor and research sites, performing site visits, verifying data accuracy, and ensuring patient safety. Their work helps ensure the integrity and reliability of clinical trial data while supporting the successful completion of research studies.

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

AspectRegional Clinical Research AssociateClinical Research Associate
Required CredentialsBachelor's degree, clinical research certification often preferredBachelor's degree, clinical research certification often preferred
Work EnvironmentTravel across multiple sites within a regionMonitor specific sites, often within a local area
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentUnderstanding regional responsibilities and scopeMonitoring specific clinical trial sites

The main difference between a Regional Clinical Research Associate and a Clinical Research Associate lies in their scope of work. The Regional CRA oversees multiple sites within a region, often traveling extensively, while the CRA typically monitors individual sites within a specific area. Both roles require similar credentials and are employed in the same industry sectors, but their geographic focus and daily responsibilities differ.

What does a regional clinical research associate do?

A regional clinical research associate works to manage studies and clinical trials associated with pharmaceutical and biotechnological drugs, products, and procedures. Your responsibilities in this career include writing and creating trial protocols, assisting in the scientific research that determines the efficacy and safety of vaccines or a medication, liaising with the ethics committee about trial subject safety, rights, and well-being, and training staff on protocol, case report form completion, and proper source documentation. Other duties include conducting research analysis, documenting and overseeing IP inventory, liaising with regulatory authorities, and tracking, managing, and ordering trial and IP materials.

Who are the top companies hiring for Regional Clinical Research Associate jobs? The top employers for Regional Clinical Research Associate jobs are:
What states have the most Regional Clinical Research Associate jobs? States with the most job openings for Regional Clinical Research Associate jobs include:
Infographic showing various Regional Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate

Icon plc

Long Beach, CA

$91K - $114K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago


Job description

Clinical Research Associate - Early Stage Development - West Region

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.


As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Focus is early-stage development clinical trials (non-oncology)
Key responsibilities include:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in a scientific or healthcare-related field.

  • Minimum of 2 years of experience as a Clinical Research Associate.

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

  • Atleast 2 years Phase I experience as a CRA within any therapeutic area.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Willingness to travel as required (approximately 65-75%) West region


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 requesthere.

Salary Range

$91,336.00-$114,170.00

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