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Clinical Research Associate Jobs in Libby, MT (NOW HIRING)

Clinical Research Coordinator

Kalispell, MT · On-site

$24 - $32/hr

Logan Health is seeking a Clinical Research Coordinator to join our research team in Kalispell ... Associate's degree in a related field * Strong communication, organization, and interpersonal ...

Clinical Research Coordinator

Kalispell, MT · On-site

$24 - $32/hr

Logan Health is seeking a Clinical Research Coordinator to join our research team in Kalispell ... Associate's degree in a related field * Strong communication, organization, and interpersonal ...

Clinical Research Associate information

See Libby, MT salary details

$10

$34

$58

How much do clinical research associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research associate in Libby, MT is $34.36, according to ZipRecruiter salary data. Most workers in this role earn between $24.09 and $43.99 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What cities near Libby, MT are hiring for Clinical Research Associate jobs?

Cities near Libby, MT with the most Clinical Research Associate job openings:

Infographic showing various Clinical Research Associate job openings in Libby, MT as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $71,478 per year, or $34.4 per hour.

Clinical Research Coordinator

Logan Health

Kalispell, MT • On-site

$24 - $32/hr

Full-time

Posted 23 days ago


Logan Health rating

6.0

Company rating: 6.0 out of 10

Based on 77 frontline employees who took The Breakroom Quiz

749th of 898 rated healthcare providers


Job description

Bring your clinical skills into a role where patient care and medical research come together.
Are you experienced in a clinical or patient-facing setting and looking for an opportunity to take the next step in your healthcare career? Logan Health is seeking a Clinical Research Coordinator to join our research team in Kalispell.
This position is a great fit for someone who enjoys working directly with patients, is confident with phlebotomy, and is interested in helping patients access new and emerging treatment options through clinical research. You don't necessarily need to come to us with every research certification already in place. We're looking for someone with a strong clinical foundation, excellent patient-care skills, attention to detail, and the ability to grow into the specialized research components of the position.
Our Mission: Quality, compassionate care for all.
Our Vision: Reimagine health care through connection, service and innovation.
Our Core Values: Be Kind | Trust and Be Trusted | Work Together | Strive for Excellence.
What You'll Do
  • Work directly with patients who may qualify for clinical research studies and help guide them through the research process
  • Screen and recruit potential study participants based on established clinical trial criteria
  • Educate patients and families about clinical studies, treatment alternatives, study requirements, and potential risks and benefits
  • Perform phlebotomy and blood collection as required for clinical research studies
  • Coordinate patient visits, testing, laboratory work, and other study-related activities
  • Build relationships with patients and serve as a consistent point of contact throughout their participation in a study
  • Collaborate with physicians, investigators, clinical staff, sponsors, and other members of the research team
  • Collect, document, and maintain accurate clinical research data
  • Help ensure studies are conducted according to established protocols, regulatory requirements, and patient safety standards
  • Coordinate multiple research studies while maintaining accurate and timely documentation

What You'll Bring
Required:
  • Associate's degree in a related field
  • Strong communication, organization, and interpersonal skills
  • Ability to work effectively with patients, families, providers, and other healthcare professionals
  • Ability to manage multiple priorities while maintaining strong attention to detail
  • Computer proficiency and the ability to learn research-specific systems and software

Preferred:
  • Bachelor's degree in a related field
  • Two years of equivalent research experience
  • Previous experience in a clinical, medical, or patient-facing environment
  • Strong phlebotomy skills and experience performing blood draws
  • Previous experience working directly with patients
  • Familiarity with medical terminology, clinical documentation, or healthcare workflows

Certifications & Training
Don't have all of the research-specific certifications yet? That's okay. Some requirements can be completed after you join the team.
  • Current Good Clinical Practice (GCP) and Human Subject Research (HSR) training is preferred at hire and must be successfully completed within 30 days of hire
  • Clinical Research certification through the Association of Clinical Research Professionals (ACRP), such as CCRC or CCRA, must be successfully obtained within three years of hire
  • Required certifications and training must be maintained throughout employment as applicable

You May Be a Great Fit If You...
  • Have worked as a Medical Assistant, Phlebotomist, CNA, clinical support professional, or in another patient-facing healthcare role
  • Are comfortable talking with patients about detailed or sensitive medical information
  • Enjoy developing relationships with patients and helping them navigate complex healthcare processes
  • Are confident performing blood draws
  • Have strong attention to detail and enjoy keeping information organized
  • Want to expand your clinical background into the growing field of clinical research
  • Enjoy being part of a collaborative team while also being able to work independently

Make an Impact Beyond the Exam Room
Clinical research brings together compassionate patient care, science, and the opportunity to advance treatment options. As a Clinical Research Coordinator, you'll help patients navigate clinical studies while working alongside providers and research professionals to support safe, high-quality research.
If you have a strong clinical foundation, enjoy working with patients, and are interested in building a career in clinical research, we encourage you to apply.
Shift:
Day Shift - 8 Hours (United States of America)
Schedule:
Logan Health operates 24 hours per day, seven days per week. Schedules are set to accommodate the requirements of the position and the needs of the organization and may be adjusted as needed.
Notice of Pre-Employment Screening Requirements
If you receive a job offer, please note all offers are contingent upon passing a pre-employment screening, which includes:
  • Criminal background check
  • Reference checks
  • Drug Screening
  • Health and Immunizations Screening
  • Physical Demand Review/Screening

Equal Opportunity Employer
Logan Health is an Equal Opportunity Employer (EOE/AA/M-F/Vet/Disability). We encourage all qualified individuals to apply for employment. We do not discriminate against any applicant or employee based on protected veteran status, race, color, gender, sexual orientation, religion, national origin, age, disability or any other basis protected by applicable law. If you require accommodation to complete the application, testing or interview process, please notify Human Resources.

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About Logan Health

Sourced by ZipRecruiter

The amazing providers, employees, and volunteers at Logan Health gift this organization with their innovation, knowledge, and compassion. Together, we're connecting our community to trusted, quality care and helping to improve lives every day.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Kalispell, MT, US

Year founded

1976