Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. This role focuses on ensuring quality oversight in clinical activities and supporting initiatives relevant to outsourced activities. The successful candidate will collaborate with key stakeholders and provide guidance on day-to-day questions arising from clinical trials deliverables.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities

• Collaborate with key stakeholders in portfolio and study teams to detect and remediate risks.
• Provide guidance on day-to-day questions arising from clinical trials deliverables.
• Interact with CROs to ensure adequate quality oversight on clinical activities.
• Collaborate with Clinical Development Operations to drive initiatives relevant to outsourced activities.
• Support inspections preparation and facilitation in collaboration with other QA groups.
• Support audits and inspections as well as follow-up activities including CAPA preparations.

Requirements

• Knowledge of Good Clinical Practice (GCP) and Quality Assurance Environment in Pharmaceutical Clinical Development or Clinical Research Organization.
• Expertise in worldwide regulations (including FDA, EMA) related to clinical development and post approval.
• An academic degree in Life Science (advanced degree preferred).

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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