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

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

Flexible working arrangements
Comprehensive healthcare plans
Life and disability insurance
Professional development support

Physician Assistant

Summary of Responsibilities

Qualifications (Minimum Required)

Experience (Minimum Required)

Preferred Qualifications

Physician Assistant

Summary of Responsibilities

Qualifications (Minimum Required)

Experience (Minimum Required)

Preferred Qualifications

Physical Demands / Work Environment

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.

Fortrea

Fortrea

Benefits

Fortrea