Part-time Physician Assistant (PA) - Phase I Site based in Daytona Beach, FL

Our phase I site based in Daytona Beach 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 Florida 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. #LI-SE1 Learn more about our EEO & Accommodations request here. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.