Sub-Investigator, Nurse Practitioner or Physician Assistant
About The Position
Headlands Research is seeking an experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator at its clinical research site in Scottsdale, Arizona. The site conducts clinical trials in CNS, psychiatry, musculoskeletal conditions, addiction, vaccines, and general medicine. The role supports clinical research delivery through technology-enabled processes and patient-centered care, while maintaining high standards of care and compliance. The position is a full-time regular employee role, performed onsite in Scottsdale, with a Monday-through-Friday schedule from 8:00 a.m. to 5:00 p.m. Pay is competitive and depends on years of experience as an investigator in clinical research and as an advanced provider. The Sub-Investigator helps ensure study participants’ safety and welfare, carries out protocol-directed assessments and care, and may provide home-based on-call availability under site policy.
Requirements
- At least two years of experience as a licensed physician assistant, family nurse practitioner, or non-acute adult nurse practitioner treating a wide variety of therapeutic areas in adult and geriatric populations; experience in internal medicine, family medicine, urgent care, or emergency medicine is specified.
- Current, unencumbered Arizona license to practice as a Nurse Practitioner or Physician Assistant.
- Commitment and ability to deliver excellent customer service.
- Excellent communication skills, punctuality, and responsibility.
- Strong organizational skills.
- Excellent verbal and written communication skills.
- Trustworthiness, reliability, and attention to detail.
- Mature and pleasant demeanor.
- Willingness to learn new tasks and grow with the company.
Nice To Haves
- Prior experience in the clinical research industry is highly preferred.
Responsibilities
- Ensure the safety and welfare of each study subject.
- Maintain in-depth knowledge of all research protocols.
- Screen potential study subjects according to protocol-specific inclusion and exclusion criteria.
- Conduct medical history interviews and physical examinations throughout subjects’ study participation.
- Review EKGs and laboratory results.
- Provide medical care as needed during a subject’s participation in a clinical trial.
- Provide home-based on-call availability per site policy.
- Attend Investigator Meetings on behalf of the Principal Investigator as needed.
- Demonstrate excellent professional communication, punctuality, and responsibility.
- Demonstrate a friendly and outgoing demeanor and a passion for direct patient interaction.
- Demonstrate clinical competence, positive leadership, and the ability to work collaboratively with a multidisciplinary team.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
