Medicine

Nevada System of Higher Education•Skokie, IL

8d•$58 - $81•Onsite

About The Position

Exciting opportunity to join Endeavor Health Research Department – Endocrinology & Metabolic Health/Medicine Team! Under the direction of the collaborating physician, the Advanced Practice Provider (APP) plays a critical role in the execution of research, including industry funded studies. This position supports research by providing protocol-driven clinical duties and assessments, ensuring regulatory compliance, and maintaining data integrity. The APP ensures participant safety while meeting sponsor timelines and performance metrics. This position will serve as a sub-investigator and/or investigator that will travel to multi-sites and support various specialties.

Requirements

Advanced Practice Licensure (APN) or Physician Assistant (PA) Licensure in the State of IL required
Federal DEA and Illinois Controlled Substance License required
Completion of Master’s level program in specialty area
BLS/CPR and ACLS certifications required
0–3+ years of experience in industry-sponsored clinical trials or clinical experience required
Excellent organizational, documentation, and time-management skills

Nice To Haves

Research experience and/or working with pharmaceutical, biotech, or device sponsors
Strong knowledge of FDA regulations and ICH-GCP
Familiarity with EDC systems (e.g., Medidata, Oracle, REDCap)
Experience with Phase I–IV clinical trials

Responsibilities

Conduct informed consent discussions and documentation per protocol
Conduct protocol-specified medical evaluations, physical exams, and eligibility assessments
Oversee study visits in accordance with sponsor protocols and schedules of events
Assess, document, and manage adverse events (AEs), serious adverse events (SAEs), and protocol deviations
Administer investigational products and study procedures
Provide ongoing medical oversight and participant education 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 in a timely manner
Support feasibility assessments, site qualification visits (SQVs), and study start-up activities
Complete all institutional and sponsor required trainings
Ensure compliance with FDA regulations, ICH-GCP guidelines, sponsor and site SOPs
Maintain accurate and contemporaneous source documentation
Support inspection readiness for internal, FDA, sponsor, and CRO audits
Accurately document clinical findings in electronic medical record (EMR), source documents, and electronic data capture (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