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Full Time Clinical Research Associate Jobs (NOW HIRING)

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Senior Clinical Research Associate

Houston, TX · Hybrid

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of ...

Eisenhower

Clinical Research Associate

Rancho Mirage, CA · On-site

$20.71 - $31.30/hr

Varies (United States of America) Hours: 40 Salary range: $20.71 - $31.30 Schedule: Full Time Shift ... Certification from Society of Clinical Research Associate (SOCRA) as a Certified Clinical Research ...

Ora

Senior Clinical Research Associate

Senior Clinical Research Associate DEPARTMENT: Monitoring Ora Values the Daily Practice of ... Benefit Eligibility: Full-time employees of Ora working a minimum of 30 hours per week. Our per ...

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Full Time Clinical Research Associate information

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$36K

$94.3K

$143.5K

How much do full time clinical research associate jobs pay per year?

As of Jun 9, 2026, the average yearly pay for full time clinical research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Full Time Clinical Research Associates when managing multiple clinical trials simultaneously?

Full Time Clinical Research Associates (CRAs) often juggle several studies at once, which can make prioritizing tasks and managing time effectively a challenge. Staying compliant with regulatory requirements while ensuring data accuracy and maintaining clear communication with site staff requires strong organizational skills. Additionally, frequent travel and adapting to different site environments can be demanding. CRAs who develop robust planning strategies and effective communication habits tend to navigate these challenges successfully, ensuring studies run smoothly and efficiently.

What is a Full Time Clinical Research Associate?

A Full Time Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials and ensuring that research studies comply with regulatory requirements and study protocols. CRAs play a critical role in the development of new drugs and medical devices by overseeing the progress of clinical trials, verifying data accuracy, and ensuring patient safety. They often travel to various clinical sites to conduct site visits, train staff, and review study documentation. Working full time, a CRA may handle multiple studies simultaneously and collaborate closely with investigators, sponsors, and regulatory agencies.

What are the key skills and qualifications needed to thrive as a Full Time Clinical Research Associate, and why are they important?

To thrive as a Full Time Clinical Research Associate, you need a solid background in life sciences or a related field, familiarity with Good Clinical Practice (GCP) guidelines, and a bachelor's degree (often required). Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and understanding of regulatory requirements is crucial, and certifications like ACRP or SOCRA are often valued. Strong attention to detail, communication, and organizational skills help you effectively monitor trials and collaborate with study sites. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, which is vital for patient safety and reliable research outcomes.

What is the difference between Full Time Clinical Research Associate vs Clinical Research Coordinator?

AspectFull Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often with clinical or life sciences background; certifications like CCRP or ACRP are commonBachelor's degree in health sciences or related field; certifications like CCRP or ACRP are also common
Work EnvironmentMonitor clinical trials at multiple sites, often traveling; work closely with sponsors and CROsManage daily trial activities at a single site; coordinate with investigators and staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites, academic institutions

While both roles require similar educational backgrounds and certifications, a Full Time Clinical Research Associate primarily monitors multiple trial sites and ensures compliance, often traveling. In contrast, a Clinical Research Coordinator manages trial activities at a single site, focusing on patient recruitment and data collection. Both roles are essential in clinical research but differ in scope and daily responsibilities.

More about Full Time Clinical Research Associate jobs
What cities are hiring for Full Time Clinical Research Associate jobs? Cities with the most Full Time Clinical Research Associate job openings:
What are the most commonly searched types of Full Time Clinical Research jobs? The most popular types of Full Time Clinical Research jobs are:
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Full Time Clinical Research Associate jobs near you
Infographic showing various Full Time Clinical Research Associate job openings in the United States as of June 2026, with employment types broken down into 76% Full Time, 9% Part Time, 2% Temporary, 11% Contract, and 2% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.
Senior Clinical Research Associate

Senior Clinical Research Associate

Icon plc

Portland, OR • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago

Job description

Contract Senior Clinical Research Associate - Home-Based (US)

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 Contract Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month contract. As a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • 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

  • Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • Minimum of 3 years independent monitoring
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to travel at least 80% of the time (international and domestic - fly and drive) and should possess a valid driver's license

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.

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

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