Part-time Physician Assistant (PA) - Phase I Site based in Madison, Wisconsin
- Location
- Madison
- Work mode
- On-site
- Employment type
- Part-time
About the job
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
- 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)
- 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.
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Learn more about our EEO & Accommodations request here .
From FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.'s careers page (Workday), checked 30 Oct 2026.
How to apply
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Posted 27 Oct 2026 · checked 30 Oct 2026 · Report this job