About The Position

The Physician Assistant provides clinical expertise and serves as a key knowledge resource on the clinical aspects of trials within Clinical Pharmacology at a Phase I site in Madison, Wisconsin. The role supports clinical study execution and may function as a sub-investigator, helping ensure participant safety, protocol adherence, and regulatory compliance. This is a part-time opportunity with a flexible work week of 20 or more hours.

Requirements

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

Nice To Haves

  • Strong communication and stakeholder engagement skills.
  • Ability to influence and collaborate across teams.
  • Demonstrated ability to drive process improvements and support change.

Responsibilities

  • Perform physical examinations, medical histories, and participant assessments as delegated by the Medical Director or 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.
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