About this role
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.
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