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Full Time Pra Clinical Research Jobs (NOW HIRING)

Horizon Clinical Research

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Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

This is a full time position. The CRA will work under the supervision of the Principal Investigator(s) and Site research manager and will include all study related activities during the clinical ...

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Full Time Pra Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 24, 2026, the average yearly pay for full time pra clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

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

AspectFull Time Pra Clinical ResearchClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree typically required; certifications like CCRP advantageous
Work EnvironmentResearch sites, hospitals, pharmaceutical companiesResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research organizations

Both roles involve managing clinical trial activities, but Full Time Pra Clinical Research often focuses on supporting clinical research protocols and data collection, while Clinical Research Coordinators handle participant recruitment, scheduling, and compliance. The roles are similar in credentials and work environment, with differences mainly in specific responsibilities.

More about Full Time Pra Clinical Research jobs

What cities are hiring for Full Time Pra Clinical Research jobs?

Cities with the most Full Time Pra Clinical Research job openings:

What are the most commonly searched types of Pra Clinical Research jobs?

The most popular types of Pra Clinical Research jobs are:

What states have the most Full Time Pra Clinical Research jobs?

States with the most job openings for Full Time Pra Clinical Research jobs include:

What job categories do people searching Full Time Pra Clinical Research jobs look for?

The top searched job categories for Full Time Pra Clinical Research jobs are:

Full Time Pra Clinical Research jobs near you
Infographic showing various Full Time Pra Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Coordinator I/II

Headlands Research

Rolling Hills Estates, CA • On-site

$25.50 - $33.75/hr

Full-time

Re-posted 19 days ago

Job description

 Rolling Hills Estates, CA
 Peninsula Research Associates (a Headlands Research site)
 Full-Time | Monday through Friday | Onsite (no opportunities for hybrid or remote)

For experienced CRCs looking for stability, collaboration, and meaningful work

If you're an experienced Clinical Research Coordinator I, or II who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, Peninsula Research Associates may be the right next step in your career.

Our Rolling Hills Estates site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research-particularly in vaccines, immunology and allergy studies.

About Peninsula Research Associates

Peninsula Research Associates (PRA) is dedicated to advancing medical treatments through the use of innovative techniques and increasing awareness. PRA has achieved significant study results in allergy, asthma, vaccines, otitis media and sinusitis treatment and has earned a reputation for conducting quality research.

Why Experienced CRCs Choose PRA
  • Multi-disciplinary collaboration with seasoned investigators and clinical staff
  • Strong operational support and clear SOPs
  • Exposure to complex, meaningful studies-not just high-volume turnover
  • A site with long-standing credibility and research maturity
  • Backing of a growing research network with resources and stability

This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision.

What You'll Do
  • Coordinate all aspects of assigned clinical trials from site initiation through close-out
  • Conduct subject visits and ensure accurate, timely documentation in compliance with ALCOA-C standards
  • Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
  • Manage subject recruitment, informed consent, and retention activities
  • Ensure timely EDC data entry and resolution of queries
  • Report and follow up on AEs, SAEs, and protocol deviations
  • Collaborate with investigators, sponsors/CROs, labs, and internal teams
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure training compliance for amendments and systems
  • Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
What We're Looking For
  • High school diploma or GED required; Bachelor's degree preferred
  • At least one full year of experience coordinating multiple Phase 2-4 industry-sponsored clinical trials required
  • Experience with regulatory, patient visits, consenting, interacting directly with sponsors, and scheduling patient visits required
  • Heavily prefer those who are trained and experienced in phlebotomy
  • Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
  • Experience with EDC, IVRS, and clinical research platforms
  • Proficiency in medical terminology and clinical documentation
  • Strong organizational skills with the ability to manage multiple studies
  • Clear, professional verbal and written communication skills
  • Comfortable working onsite in a collaborative, clinical environment
Who Thrives in This Role
  • CRCs who want structure, support, and accountability
  • Professionals who value teamwork over silos
  • Coordinators who care about data quality, patient experience, and compliance
  • Those ready to grow within a stable, well-established research site

 Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.

Apply