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

As of Aug 11, 2026, the average yearly pay for full time clinical research organization 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 are the key skills and qualifications needed to thrive in a full time clinical research organization role?

Excelling in a Full-Time Clinical Research Organization role requires a solid background in life sciences, understanding of clinical trial protocols, and often a relevant degree such as in biology, pharmacology, or nursing. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are typically expected. Strong attention to detail, communication, and organizational skills help professionals effectively manage studies and collaborate with diverse stakeholders. These skills and qualifications are crucial for ensuring trial integrity, regulatory compliance, and successful research outcomes.

What are some common challenges faced when working full time at a clinical research organization (CRO)?

Working full-time at a Clinical Research Organization can be both rewarding and demanding. Common challenges include managing multiple studies simultaneously, adapting to evolving regulatory requirements, and meeting tight project deadlines. Team members often collaborate across departments—such as data management, regulatory affairs, and clinical operations—which requires strong communication and organizational skills. Navigating these challenges successfully provides valuable experience and opportunities for career growth within the clinical research field.

What is a clinical research organization (CRO)?

A Clinical Research Organization (CRO) is a company that provides support to pharmaceutical, biotechnology, and medical device industries by offering research services outsourced on a contract basis. These organizations help manage and conduct clinical trials, handle regulatory affairs, data management, and ensure compliance with Good Clinical Practice (GCP). CROs play a crucial role in bringing new drugs and treatments to market more efficiently by streamlining the research process and reducing costs for sponsors. Full-time positions in a CRO can include roles in clinical operations, project management, data analysis, and quality assurance. Working in a CRO provides exposure to a variety of clinical trials and therapeutic areas.
What cities are hiring for Full Time Clinical Research Organization jobs? Cities with the most Full Time Clinical Research Organization job openings:
What are the most commonly searched types of Clinical Research Organization jobs? The most popular types of Clinical Research Organization jobs are:
What states have the most Full Time Clinical Research Organization jobs? States with the most job openings for Full Time Clinical Research Organization jobs include:
Full Time Clinical Research Organization jobs near you

Clinical Research Coordinator

Rocky Mountain Clinical Research

Idaho Falls, ID • On-site

$17 - $25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 days ago

Job description

Clinical Research Coordinator (Full-Time)
Rocky Mountain Clinical Research Idaho Falls, ID
Rocky Mountain Clinical Research is seeking a full-time Clinical Research Coordinator (CRC) to join our growing team in Idaho Falls, ID. This is an excellent opportunity for a healthcare professional looking to expand into clinical research while making a meaningful impact on patient care and the future of medicine.
If you enjoy working directly with patients, value precision and organization, and want to be part of a collaborative, mission-driven research organization, we encourage you to apply.
Compensation & Benefits
  • Hourly wage: $17 - $25 per hour (based on education, training, and experience)
  • Benefits package includes:
    • Medical, dental, and vision insurance
    • 401(k) retirement plan
    • Paid time off (PTO)
  • Full-time, stable position with opportunities for professional growth

About Rocky Mountain Clinical Research
Rocky Mountain Clinical Research was founded on the principle of advancing medical care for patients facing complex diseases. We conduct high-quality clinical research across a range of therapeutic areas, including diabetes, evaluating medications and medical devices to determine their safety and effectiveness compared to current standards of care.
As an investigator-led, patient-focused research site, we play a key role in bringing new treatments to market while ensuring patient safety and regulatory compliance. We are a family-oriented organization that values teamwork, integrity, and long-term employee success.
Position Summary: Clinical Research Coordinator
The Clinical Research Coordinator plays a critical role in the day-to-day execution of clinical trials. Working closely with the Principal Investigator, Research Director, and study team, the CRC ensures that clinical studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), and federal regulations.
This role combines patient interaction, clinical coordination, and administrative responsibilities, making it ideal for detail-oriented healthcare professionals who enjoy both people-facing and organizational work.
Key Responsibilities
  • Coordinate and administer clinical trials under the direction of the Principal Investigator
  • Screen, enroll, consent, and follow study participants
  • Ensure participant safety and protocol adherence throughout the study lifecycle
  • Maintain accurate source documentation and regulatory files
  • Complete study-related data entry and follow-up documentation with high attention to detail
  • Prepare for and support sponsor, monitor, and regulatory audits
  • Collaborate with investigators, sponsors, monitors, and internal research staff
  • Ensure studies are conducted in compliance with GCP, FDA regulations, and study protocols

Required Qualifications
  • Healthcare or medical background (clinical or patient-facing experience)
  • Strong clerical, organizational, and documentation skills
  • Excellent interpersonal and communication skills
  • High attention to detail and commitment to quality and accuracy
  • Ability to work independently while collaborating effectively with a team

Preferred Qualifications
  • Certified Medical Assistant (CMA), Licensed Practical Nurse (LPN), Registered Nurse (RN), or higher credentialing
  • Experience in a healthcare, research, or clinical trial environment
  • Familiarity with Good Clinical Practice (GCP), clinical trial protocols, or regulatory documentation
  • Strong analytical and decision-making skills

Clinical research experience is preferred but not required- GCP and CRC training will be provided for motivated candidates.
Work Schedule
  • Full-time
  • Monday - Friday
  • Occasional (but rare) weekends or major holidays required

Ready to Join Our Team?
If you're passionate about patient care, clinical excellence, and contributing to the future of medicine, we'd love to hear from you. Join our team of 25 Clinical Research Coordinators where your work truly makes a difference.
Apply today to become part of Rocky Mountain Clinical Research.
We understand your time is valuable, so we have a very quick and easy application process. If you feel that you have the right medical or nursing background for this clinical study job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
Location: 83404

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