Nurse Practitioner or Physician Assistant

<div class="content-intro"><p>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</p></div><p><strong>Championing Diversity in Clinical Trials</strong></p> <p>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.</p> <p>&nbsp;</p> <p><strong>The Role of a Lifetime</strong></p> <p>Are you ready to make a difference? We're seeking an experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator to help us grow our clinical research site located in Stockbridge, GA. <strong>The site is expanding our therapeutic areas to include CNS related conditions. We are ideally seeking an advanced provider with experience working in this space.</strong></p> <p>Clinical Research Atlanta, a Headlands Research site, is a leading multi-specialty research center with a long-standing reputation for excellence. The site has delivered more than 300 clinical trials across a wide range of therapeutic areas, including addiction, dermatology, infectious diseases, and more.&nbsp;</p> <p>&nbsp;</p> <p><strong>Type:</strong>&nbsp; Part Time Employee, Flexible Schedule&nbsp;</p> <p><strong>Pay:</strong>&nbsp; Competitive and dependent upon years of experience as an Investigator in clinical research.&nbsp;</p> <p><strong>Location:&nbsp;</strong> Onsite in Stockbridge, GA (no opportunities for remote or hybrid)</p> <p><strong>Schedule:&nbsp;</strong> (Part Time) within Mondays through Thursdays, 7:30am - 5:30pm</p> <p>&nbsp;</p> <p><strong>Responsibilities:</strong></p> <ul> <li>Ensure the safety and welfare of each study subject</li> <li>Have in-depth knowledge of all research protocols</li> <li>Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria</li> <li>Conduct medical history interviews and physical examinations throughout the subject’s study participation</li> <li>Review EKG’s and lab results</li> <li>Provide medical care as needed during a subject’s participation in a clinical trial</li> <li>Provide home based on-call