Nurse Practitioner - Plymouth, MA - Clinical Research
About The Position
Headlands Research Eastern Massachusetts, in partnership with Seacoast Neurology Group, is seeking an experienced Nurse Practitioner or Physician Assistant to join our growing clinical research team as a Sub-Investigator in Plymouth, Massachusetts. This role is ideal for an advanced provider who is passionate about caring for adult and geriatric patients - particularly those affected by Alzheimer’s disease, dementia, and other neurological conditions - and who wants to play a direct role in advancing future treatments through clinical research. We are especially interested in connecting with providers who live within a commutable distance to Plymouth and who value building strong relationships with patients and caregivers in a collaborative, patient-centered environment. Headlands Research is a leading integrated clinical trial site network with a mission to improve lives by advancing innovative medical therapies. Our sites partner with sponsors and CROs to conduct high-quality clinical trials across a variety of therapeutic areas while delivering exceptional patient care and operational excellence. At our Eastern Massachusetts site, we are proud to partner closely with Seacoast Neurology Group to advance neurological and dementia-focused research within the local community.
Requirements
- Minimum of 2 years of experience as a licensed Nurse Practitioner or Physician Assistant preferred; willing to consider new graduates
- Current and unencumbered NP or PA license in the state of Massachusetts required
- Experience working with adult and geriatric patient populations required
- Prior experience caring for patients with dementia, Alzheimer’s disease, neurology, geriatrics, psychiatry, primary care, or related specialties strongly preferred
- Clinical research experience preferred, but not required
- Strong interpersonal skills with the ability to communicate effectively with cognitively impaired patients and caregivers
- Highly organized with strong attention to detail
- Professional, dependable, and collaborative demeanor
- Passion for direct patient interaction and advancing medical research
- Ability to thrive in a fast-paced, team-oriented clinical environment
Responsibilities
- Ensure the safety and welfare of clinical trial participants
- Conduct medical history reviews and physical examinations
- Evaluate potential study participants according to protocol inclusion/exclusion criteria
- Review EKGs, laboratory results, and other clinical assessments
- Provide medical oversight and care throughout study participation
- Develop strong rapport with dementia patients and caregivers through compassionate communication
- Collaborate closely with neurologists, research coordinators, and sponsor representatives
- Maintain in-depth knowledge of assigned research protocols
- Attend Investigator Meetings on behalf of the Principal Investigator as needed
- Support high-quality data collection and protocol compliance
- Demonstrate professionalism, accountability, and strong patient-centered communication
Benefits
- Health insurance
- Dental insurance
- Vision insurance
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
