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Clinical Research Assistant Jobs in Rigby, ID (NOW HIRING)

Sevita Health

Clinical Coordinator

Idaho Falls, ID · On-site

$47K/yr

Clinical Coordinator - IDD Services Idaho Falls, ID Full Time Salary: $47,800/yr Looking for ... Attend staff meetings and interdisciplinary team meetings as needed. * Assist with socialization ...

IQVIA

MedTech Field Service Technician

Idaho Falls, ID · On-site

Perform bi-annual or yearly preventative maintenance as determined by the customer. * Assist in the ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

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How much do clinical research assistant jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical research assistant in Rigby, ID is $19.47, according to ZipRecruiter salary data. Most workers in this role earn between $14.86 and $22.26 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are the key skills and qualifications needed to thrive as a clinical research assistant?

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.
More about Clinical Research Assistant jobs

What cities near Rigby, ID are hiring for Clinical Research Assistant jobs?

Cities near Rigby, ID with the most Clinical Research Assistant job openings:

Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Rigby, ID as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 20% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $40,506 per year, or $19.5 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 28 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

Apply