Physician Assistant - Clinical Research

Headlands Research

Chesterfield, MOFull-timePosted Mar 31, 2026

Behavioral Health Market Context

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Job Description

hampioning Diversity in Clinical Trials

Diversity isn't just a checkbox for us - it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking an experienced Physician Assistant or Nurse Practitioner to help us grow our clinical research site located in the Greater St. Louis Area. You will help the site conduct clinical research trials involving gastroenterology, neurology, vaccines, and general internal medicine.

Clinical Research Professionals (CRP) is a dedicated research center that provides a network of providers who work collaboratively in conducting clinical research trials. The site's team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.

Type: Full-time Regular Employee

Pay: Competitive and dependent upon years of experience as an Investigator in clinical research.

Location: Onsite in Chesterfield, MO (no opportunities for remote or hybrid)

Schedule: Mondays through Fridays, 8:00am-5:00pm

Responsibilities:
• Ensure the safety and welfare of each study subject
• Have in-depth knowledge of all research protocols
• Screen potential study subjects according to the protocol's specific inclusion and exclusion criteria
• Conduct medical history interviews and physical examinations throughout the subject's study participation
• Review EKG's and lab results
• Provide medical care as needed during a subject's participation in a clinical trial
• Provide home based on-call availability per standard policy
• Attend Investigator Meetings on behalf of Principal Investigator as needed
• Excellent professional communication, punctual and responsible
• Friendly and outgoing demeanor
• Must demonstrate a passion for direct patient interaction
• Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team

Qualifications:
• Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
• Current and unencumbered license to practice as an PA or NP in the state of Missouri required
• Prior experience within the clinical research industry highly preferred
• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremely well organized
• Excellent verbal and written communication skills
• Trustworthy, reliable; attentive to details
• Mature and pleasant demeanor
• Willingness to learn new tasks and grow with the company

Qualifications

  • Friendly and outgoing demeanor
  • Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
  • Current and unencumbered license to practice as an PA or NP in the state of Missouri required
  • Commitment and ability to deliver excellent customer service
  • Excellent communication, punctual and responsible
  • Extremely well organized
  • Excellent verbal and written communication skills
  • Trustworthy, reliable; attentive to details
  • Mature and pleasant demeanor
  • Willingness to learn new tasks and grow with the company

Benefits

  • Pay: Competitive and dependent upon years of experience as an Investigator in clinical research
  • Schedule: Mondays through Fridays, 8:00am-5:00pm

Responsibilities

  • Type: Full-time Regular Employee
  • Ensure the safety and welfare of each study subject
  • Have in-depth knowledge of all research protocols
  • Screen potential study subjects according to the protocol's specific inclusion and exclusion criteria
  • Conduct medical history interviews and physical examinations throughout the subject's study participation
  • Review EKG's and lab results
  • Provide medical care as needed during a subject's participation in a clinical trial
  • Provide home based on-call availability per standard policy
  • Attend Investigator Meetings on behalf of Principal Investigator as needed
  • Excellent professional communication, punctual and responsible
  • Must demonstrate a passion for direct patient interaction
  • Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team


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