Advanced Practice Provider (APN/PA) - Research - Endocrinology/Metabolic Health/ Medicine

Hourly Pay Range $57.76 - $80.86 Position Advanced Practice Provider (APN/PA) – Research – Diabetes, Obesity, Cardiometabolic, and Medicine Health Research Location 9977 Woods Drive, Skokie, IL Hours Monday through Friday, 8:00AM – 4:30PM, with occasional early morning or evening hours. Full-time (average 40 hours per week). Travel Occasional travel to other NorthShore sites; attendance at out-of-state investigator conferences 3–4 times per year is highly encouraged. Job Description Under the direction of a collaborating physician investigator, perform protocol‑driven clinical duties and assessments to execute industry‑funded studies. Provide participant safety, meet sponsor timelines, and uphold performance metrics as a sub‑investigator or investigator across multiple sites. Conduct informed consent discussions and documentation per protocol. Perform protocol‑specified medical evaluations, physical examinations, eligibility assessments, and other clinical procedures (phlebotomy, IV insertion, infusions, etc.). Build trusting relationships with study participants to promote recruitment, retention, and long‑term adherence. Oversee study visits in accordance with sponsor protocols and schedule of events. Assess, document, and manage adverse events, serious adverse events, and protocol deviations. Administer investigational products and study procedures. Provide ongoing medical oversight and education to participants throughout trial participation. Collaborate with study monitors, sponsors, and CRO representatives during monitoring visits and audits. Respond to sponsor queries, data clarifications, and safety follow‑ups promptly. Support feasibility assessments, site qualification visits, and study start‑up activities. Complete all institutional and sponsor required trainings. Ensure compliance with FDA regulations, ICH‑GCP guidelines, sponsor and site SOPs, and local regulations and ethical standards. Maintain accurate and contemporaneous source documentation. Support inspection readiness for internal, FDA, sponsor, and CRO audits. Accurately document clinical findings in EMR, source documents, and EDC systems. Collaborate with research coordinators to resolve data discrepancies and queries. Ensure real‑time documentation to meet sponsor data lock timelines. Work closely with Principal Investigator, Sub‑Investigators, Research Management, and research staff. Serve as a clinical resource for protocol interpretation and medical decision‑making. Communicate participant safety issues and protocol concerns to sponsors and CROs. Participate in team meetings, institutional events, sponsor conferences, and trainings. Contribute to the advancement of medicine by helping bring innovative therapies and technologies to patients. Build meaningful, long‑term relationships with study participants and support them throughout their research journey. Work collaboratively with multidisciplinary teams, including physicians, nurses, dietitians, coordinators, and industry partners. Qualifications Advanced Practice Licensure (APN) or Physician Assistant (PA) Licensure in the State of Illinois. Federal DEA and Illinois Controlled Substance License. Completion of a Master’s‑level program in a specialty area. BLS/CPR and ACLS certifications. 0–3+ years of experience in industry‑sponsored clinical trials or clinical experience. Excellent organizational, documentation, and time‑management skills. Preferred: Research experience and/or working with pharmaceutical, biotech, or device sponsors. Knowledge of FDA regulations and ICH‑GCP. Familiarity with EDC systems (e.g., Medidata, Oracle, REDCap). Experience with Phase I–IV clinical trials. Benefits Career Pathways to Promote Professional Growth and Development. Various Medical, Dental, and Vision options. Health Savings Account options. Wellness Program. Savings Plan. Tuition Reimbursement. Free Parking at designated locations. Retirement Options with Company Match. Paid Time Off and Holiday Pay. Community Involvement Opportunities. CME allowance. EEO Statement Endeavor Health is an Equal Opportunity Employer: Race/Color/Sex/ Sexual Orientation/ Gender Identity/ Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor. #J-18808-Ljbffr 1100 Endeavor Health Clinical Operations