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

Fortrea Development India Private Limited; Madison (WI); On-site; USD 55,000 - 83,000; Part time

Job summary

Fortrea Development India Private Limited in Madison, WI, seeks a Part-time Physician Assistant to provide clinical expertise for early-phase clinical pharmacology trials. You will support study execution, ensure participant safety, and help maintain regulatory compliance at a dedicated phase I site in Madison.

The role requires PA-C with Wisconsin licensure, 3–5 years of clinical experience, and strong English communication.

Qualifications

• Graduate of an accredited Physician Assistant program.
• Current PA-C certification via NCCPA with Wisconsin license.
• Equivalent education and experience may be considered where applicable.
• Strong English communication skills (written and verbal).

Responsibilities

• Perform physical examinations, medical histories, and participant assessments as delegated by medical leadership.
• Review screening data and lab results to assess participant eligibility.
• Interact with regulatory bodies as relevant to clinical operations.
• Serve as a technical advisor to clinical teams and cross-functional partners.
• Support development and improvement of operational processes and clinical facilities.
• Participate in clinical feasibility assessments for new study proposals.
• Ensure compliance with FDA, GCP, and ICH regulations.
• Attend investigator meetings and serve as an educational resource for staff.

Skills

Clinical communication

Stakeholder engagement

Process improvement

Team collaboration

Education

PA program graduate

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 proposalsOversee 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.