Sub-Investigator, Nurse Practitioner or Physician Assistant

Headlands Research•Scottsdale, AZ

21h•Onsite

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 and patient-centered care while following study protocols and compliance standards. The position is a regular, full-time employee role, 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 a clinical research Investigator and as an advanced provider. Remote and hybrid work are not available. Headlands Research operates clinical trial sites in the United States and Canada and describes diversity and inclusion as central to its mission. The Scottsdale site partners with pharmaceutical sponsors and CROs to advance therapies and uses technology to streamline research processes for partners and study participants. Headlands Research is an Equal Opportunity Employer and will provide reasonable accommodation during the application process for individuals with disabilities. The company states that it will not request personal identifying information or a financial deposit through email or messaging tools.

Requirements

At least two years of experience as a licensed physician assistant, family nurse practitioner, or non-acute adult nurse practitioner treating adult and geriatric patients across a wide variety of therapeutic areas; examples include internal medicine, family medicine, urgent care, and emergency medicine.
Current, unencumbered Arizona license to practice as a Nurse Practitioner or Physician Assistant.
Commitment and ability to deliver excellent customer service.
Excellent verbal and written communication skills.
Strong organization and attention to detail.
Trustworthiness and reliability.
Mature and pleasant demeanor.
Willingness to learn new tasks and grow with the company.
Friendly and outgoing demeanor, with a passion for direct patient interaction.

Nice To Haves

Prior experience within 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 each protocol’s 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 in accordance with site policy.
Attend Investigator Meetings on behalf of the Principal Investigator as needed.
Demonstrate professional communication, punctuality, and responsibility.
Work collaboratively with a multidisciplinary team and demonstrate clinical competence and positive leadership.