Research Medical Assistant

Northeast Healthcare Recruitment, Inc. (NEHCR)

Casper, WYFull-timePosted Apr 9, 2026

Behavioral Health Market Context

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Job Description

ition, with a flexible schedule based on clinic and study needs.

Compensation: $27.50–$29.00 Per Hour
Responsibilities
• Support clinical trials in compliance with IRB, federal, and state regulations
• Assist with patient visits, intake, vitals, and documentation
• Schedule tests, referrals, and obtain pre-authorizations
• Screen and recruit study participants per protocol requirements
• Administer study medications and monitor for side effects
• Educate patients on treatments and study protocols
• Maintain accurate and timely medical records
• Collaborate with providers to ensure continuity of care
• Respond to emergencies and assist with CPR if needed
• Participate in training, staff meetings, and required certifications
• Assist with onboarding and training of new staff
Requirements
• High school diploma or equivalent (Medical Assistant certification preferred)
• Prior medical assistant or clinical research experience preferred
• Knowledge of clinical research protocols and patient care practices
• Current BLS/CPR certification

Located in Casper, this vibrant city offers a mix of outdoor adventure and small-town charm. Nestled along the North Platte River, Casper is known for its scenic landscapes, nearby hiking and skiing, and a strong sense of community, making it a great place to live and work.

Qualifications

  • Knowledge of clinical research protocols and patient care practices
  • Current BLS/CPR certification

Benefits

  • Compensation: $27.50–$29.00 Per Hour

Responsibilities

  • Seeking a Part-Time Research Medical Assistant (MA) to support clinical trials in Casper, WY by ensuring compliance with protocols, regulatory requirements, and patient safety standards while delivering high-quality patient care
  • This role serves as a key liaison between providers, patients, and the care team, assisting with clinical data collection and patient flow
  • This is a 20-hour per week position, with a flexible schedule based on clinic and study needs
  • Support clinical trials in compliance with IRB, federal, and state regulations
  • Assist with patient visits, intake, vitals, and documentation
  • Schedule tests, referrals, and obtain pre-authorizations
  • Screen and recruit study participants per protocol requirements
  • Administer study medications and monitor for side effects
  • Educate patients on treatments and study protocols
  • Maintain accurate and timely medical records
  • Collaborate with providers to ensure continuity of care
  • Respond to emergencies and assist with CPR if needed
  • Participate in training, staff meetings, and required certifications
  • Assist with onboarding and training of new staff


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