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

FTCRUMAD Fortrea Clinical Research Unit Inc.; United States; Sur place; USD 83 000 - 124 000; Temps partiel

Résumé du poste

Fortrea Clinical Research Unit Inc. in Madison, WI is seeking a Part-Time Physician Assistant to provide clinical expertise for early-phase trials within Clinical Pharmacology.

The role may function as a sub-investigator, ensuring participant safety, protocol adherence, and regulatory compliance. The position supports the execution of clinical studies, serves as a clinical resource and trainer for staff, and may require some overtime or weekend work as needed.

Qualifications

• Graduate of an accredited Physician Assistant program.
• Current PA-C certification via NCCPA with Wisconsin state licensure.
• 3–5 years of relevant clinical experience.
• Strong English communication skills (written and verbal).

Responsabilités

• 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.

Connaissances

English communication

Formation

PA-C credential (NCCPA)

Description du poste

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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