What are the responsibilities and job description for the Part-time Physician Assistant (PA) - Phase I Site based in Madison, Wisconsin position at Fortrea?
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
- 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.
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.