Physician Assistant

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Leeds, West Yorkshire, England, GBR
In-Office
Biotech
The Role

Job Overview:

The Physician Assistant will provide an information service and knowledge base on the clinical aspects of clinical trials in Clinical Pharmacology. In addition, he/she may act as a sub-investigator.

    Summary of Responsibilities:

    • Perform physical examinations/medical histories, and other participant assessments as delegated by the Medical Director/Associate Medical Director.
    • Review screening data including laboratory data and assess participant eligibility to check-in to the unit for clinical trials.
    • Interact with regulatory bodies as are relevant to the operations department.
    • Assume responsibility as technical advisor to the clinical teams and other departments within Clinical Pharmacology.
    • Maintain and further develop facilities and processes relevant to operations.
    • May perform clinical feasibility review of new proposals.
    • Oversee and direct the development/implementation of quality systems to ensure good clinical practices are maintained.
    • Ensure compliance with FDA/GCP/ICH regulations.
    • Perform routine study activities as needed.
    • May assist operations and client managers with Sponsor visits and interactions as appropriate.
    • Ensure safe working practices/environment is employed and maintained.
    • Recommend changes as necessary and justify them in accordance with company policy.
    • Attend investigator meetings as appropriate.
    • Serves as an educational resource and instructor/trainer for staff.
    • And all other duties as needed or assigned.

    Qualifications (Minimum Required):

    • UK: Post Graduate Diploma/MSc Physician Associate Studies or equivalent.
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

    Experience (Minimum Required):

    • 3 to 5 years minimum relevant experience.

    Preferred Qualifications Include:

    • Ability to communicate information.
    • Ability to negotiate daily with internal stakeholders.
    • Ability to effect change where persuasion is required.

    Physical Demands/Work Environment:

    • Requires the handling of biological and/or hazardous or radioactive material.
    • Must be able to see (distinguish colors) and hear.
    • Must have an excellent command of the English language, both oral and written.
    • Must be able to use hands to finger, handle, or touch objects, tools, or controls, including a computer keyboard, for up to 6 hours per day.
    • Must be able to stand and/or bend for up to 6 hours per day.
    • Overtime and weekend work as required.

    Learn more about our EEO & Accommodations request here.

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    The Company
    HQ: Research Triangle Park, NC
    10,811 Employees

    What We Do

    Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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