Part-time Physician Assistant (PA) - Phase I Site based in Madison, Wisconsin

Our phase I site based in Madison is looking for a PART TIME Physician Assistant to provide clinical expertise and serves as a key knowledge resource on the clinical aspects of trials within Clinical Pharmacology. This role supports the execution of clinical studies and may function as a sub-investigator, ensuring participant safety, protocol adherence, and regulatory compliance. Summary of Responsibilities - Perform physical examinations, medical histories, and participant assessments as delegated by the Medical Director/Associate Medical Director - Review screening data, including laboratory results, to assess participant eligibility for clinical trial check-in - Interact with regulatory bodies as relevant to clinical operations - Serve as a technical advisor to clinical teams and cross-functional partners within Clinical Pharmacology - Support the development and continuous improvement of operational processes and clinical facilities - Participate in clinical feasibility assessments for new study proposals - Oversee and contribute to the development and implementation of quality systems to ensure compliance with Good Clinical Practice (GCP) - Ensure adherence to FDA, GCP, and ICH regulations - Perform routine study-related activities as required - Support Sponsor visits and interactions in partnership with operations and client management - Maintain a safe work environment and recommend improvements aligned with company policy - Attend investigator meetings as appropriate - Serve as an educational resource and trainer for staff - Perform additional duties as assigned Qualifications (Minimum Required) - USA: Graduate of an accredited Physician Assistant program - Current certification as a Physician Assistant (PA-C) via NCCPA - with state of Wisconsin - Equivalent education and experience may be considered where applicable - Strong English communication skills (written and verbal) Experience (Minimum Required) - 3–5 years of relevant clinical experience Preferred Qualifications - Strong communication and stakeholder engagement skills - Ability to influence and collaborate across teams - Demonstrated ability to drive process improvements and support change Physical Demands / Work Environment - Work is performed in a clinical and/or laboratory environment with potential exposure to biological, hazardous, or radioactive materials - Ability to see (distinguish colors) and hear clearly - Ability to perform repetitive hand and computer-based tasks for extended periods (up to 6 hours/day) - Ability to stand, walk, and bend for extended periods (up to 6 hours/day) - Flexibility to work overtime or weekends as needed This part-time opportunity offers the flexibility of a 20+ hour work week while providing meaningful exposure to early-phase clinical research, collaboration with experienced medical teams, and the opportunity to expand your clinical and research expertise. #LI-SE1 Learn more about our EEO & Accommodations request here.