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Full Time H1B Clinical Research information

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$49K

$107.3K

$189K

How much do full time h1b clinical research jobs pay per year?

As of Sep 7, 2026, the average yearly pay for full time h1b 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 a full time H1B clinical research position?

A Full Time H1B Clinical Research position refers to a clinical research job in the United States that is filled by an employee who is sponsored under the H1B visa program. This allows qualified foreign professionals, typically with a background in science or medicine, to work legally in the U.S. on clinical research projects. The position is considered full time, meaning the employee works the standard number of weekly hours set by the employer, and the job entails conducting, managing, or supporting clinical trials and research studies. Employers must meet certain requirements to sponsor an H1B visa, including demonstrating that the job requires specialized knowledge.

What are some common challenges faced by H1B clinical research professionals working full-time in the U.S.?

Full-time H1B Clinical Research professionals often navigate challenges such as adapting to new regulatory environments, managing complex documentation for both clinical trials and visa compliance, and balancing the demands of rigorous study protocols with tight timelines. Additionally, collaboration with multidisciplinary teams requires strong communication skills, especially when working with colleagues from diverse backgrounds. Many also find the need to stay up-to-date with evolving FDA and IRB requirements, which can be demanding but is essential for career advancement.

What are the key skills and qualifications needed to thrive as a full time H1B clinical research professional, and why are they important?

To thrive as a Full Time H1B Clinical Research professional, you typically need a degree in life sciences or a related field, experience with clinical trials, and eligibility to work under H1B sponsorship. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are often required. Strong organizational skills, attention to detail, and the ability to communicate effectively with cross-functional teams set candidates apart. These skills and qualifications are crucial for ensuring regulatory compliance, data integrity, and the successful execution of clinical studies.
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Cities with the most Full Time H1B Clinical Research job openings:

What are the most commonly searched types of H1B Clinical Research jobs?

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What states have the most Full Time H1B Clinical Research jobs?

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Full Time H1B Clinical Research jobs near you
Infographic showing various Full Time H1B Clinical Research 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 $107,336 per year, or $51.6 per hour.

Clinical Research Coordinator

Rocky Mountain Clinical Research

Idaho Falls, ID • On-site

$17 - $25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 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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