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

Fortrea; Madison (WI); On-site; USD 60,000 - 80,000; Part time

Job summary

Fortrea Madison seeks a part-time Physician Assistant to contribute to early-phase clinical trials within Clinical Pharmacology. You will conduct exams, reviews, and participant assessments under the Medical Director, ensuring safety and protocol compliance.

This role offers valuable exposure to trial operations, regulatory processes, and collaboration with cross-functional teams while maintaining a flexible 20+ hour work week.

Qualifications

• Licensed Physician Assistant (PA-C) with current certification
• Graduate of an accredited Physician Assistant program
• Experience working in clinical trials or related healthcare settings preferred
• Strong English communication skills (written and verbal)

Responsibilities

• Perform physical examinations, medical histories, and participant assessments as delegated by the Medical Director/Associate Medical Director
• Review screening data and laboratory results to determine participant eligibility for 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 development and continuous improvement of operational processes and clinical facilities
• Oversee and contribute to quality systems to ensure compliance with GCP
• Ensure adherence to FDA, GCP, and ICH regulations
• Attend investigator meetings and provide educational resources and training for staff

Job description

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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