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Full Time Clinical Research Associate Jobs (NOW HIRING)

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 innovative ...

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$143.5K

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

As of Aug 11, 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?

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 August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Research Associate - (Oncology)

UPMC Senior Communities

Pittsburgh, PA • On-site

$24.32 - $40.54/hr

Full-time

Re-posted 15 days ago

Job description

Purpose:
UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Associate - Oncology to help support the Clinical Research Services team located within the Hillman Cancer Center in Shadyside/Pittsburgh, PA & Hillman Women's Oncology Program at Magee Women's Hospital in Oakland/Pittsburgh, PA. This role will float and support various Oncology Disease Center program studies working Monday through Friday daylight hours.
The Clinical Research Services (CRS) team is made up of nearly 200 staff members who facilitate development, implementation, coordination, internal data monitoring, and completion of oncology-focused trials at Hillman. These trials include institutional (investigator-initiated), multi-center cooperative group/National Clinical Trial Network (NCTN), consortium, and industry-sponsored trials. Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
Under the direction of the Clinical Research Manager, the research associate will work with physicians, nurses, and allied health professionals to facilitate clinical research trials provided through the University of Pittsburgh Cancer Institute (UPCI) and UPMC Hillman Cancer Centers and to independently execute job functions related to protocol management.
This position is part of a UPMC Research Career ladder. The incumbent will be hired into the appropriate level of research associate position based on their current education and experience level.
Responsibilities:
  • Assists in entering subject trial registration and study status updates into CTMA.
  • Assists in the coordination of initiation, site evaluation, monitoring visits, and audits required by the sponsor.
  • Assists in verifying subject eligibility according to protocols by reviewing medical records, laboratory, and radiology or CT scan results.
  • Create study-specific source documents, case report forms and study visit checklists.
  • Ensures that patient's records, slides, radiology tests, lab work results, etc. are obtained and reviewed prior to patient entry into a study.
  • Performs consenting process and study implementation of lab, registry, and non-therapeutic clinical trials.
  • Process required documents as need for the research protocols.
  • Responsible for prompt and accurate data collection for protocols.
  • Shares responsibility of managing the day-to-day activities for the research protocols.
  • Will serve as an assistant to support all main functions of the department.

Qualifications:
Qualifications:
  • High school diploma or equivalent required.
  • Bachelor's degree in healthcare or related field
    • OR four (4) years of experience in clinical research and/or related setting
    • OR three (3) years of experience in clinical research with certification.
  • Additional skills include prior knowledge and use of Microsoft Office software produces and the ability to work with a PC database application.
  • Preferred knowledge of research methodology and prior supervisory and or/ project management experience preferred.
  • Oncology and/or Research experience preferred.

Licensure, Certifications, and Clearances:
  • Act 34 Criminal Clearance

UPMC is an equal opportunity employer. Minority/Females/Veterans/Individuals with Disabilities

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