Clinical Quality Assurance Specialist (GCP)

Philogen S.p.A.; Siena; In loco; EUR 45.000 - 65.000; Tempo pieno

Descrizione del lavoro

A leading biopharmaceutical company in Tuscany is seeking a Clinical Quality Assurance Specialist (GCP). This role involves managing compliance with GCP, conducting audits, and training staff. The ideal candidate should have a background in Life Sciences and 3-5 years of clinical QA experience. This is a unique opportunity to contribute to high-quality clinical trials in a dynamic environment.

Competenze

• 3-5 years of experience in Clinical Quality oversight.
• Understanding of clinical research principles and practices.
• High level of English proficiency.

Mansioni

• Maintain GCP/ICH compliant systems and processes.
• Write and review clinical SOPs.
• Manage training of staff on GCP regulations.
• Perform internal audits and checks to ensure compliance.

Conoscenze

Knowledge of GCP/ICH

Attention to detail

Excellent interpersonal skills

Independent work ability

Flexibility in changing tasks

Formazione

MSc. in Biology, Biotechnology, Life Sciences

Descrizione del lavoro

Clinical Quality Assurance Specialist (GCP)

Philogen is looking for a "Clinical Quality Assurance Specialist (GCP)". The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with other functions in the Clinical Department.

The successful candidate will be responsible to:

• Maintain GCP/ICH compliant systems and processes which control the quality of work and clinical trials conducted in Europe and US.
• Write and/or review clinical SOPs and support continuous process improvements.
• Manage training of staff on company procedures, GCP regulations, and documentation systems.
• Qualify CRO and other vendors related to the clinical activity.
• Perform documentation control in the TMF and quality reviews of clinical trial essential documents and associated documentation (including Protocols, Investigator’s Brochure, CRFs, etc.) as appropriate.
• Perform routine internal System and TMF audits and checks throughout the lifecycle of a trial/program to ensure compliance with internal procedures, as well as regulatory guidelines.
• Report significant clinical quality deficiencies and/or risks to upper management and actively participate in solving the issues.
• Perform clinical site GCP auditing activities to ensure that studies are conducted in accordance with sponsor protocols, GCP, industry guidelines, and agency regulations.
• Lead role to prepare company and clinical sites for customer audits and regulatory GCP inspections. Participate as Subject Matter Expert during regulatory GCP inspections.

The ideal candidate should have:

• A good scientific background (ideally MSc. in Biology, Biotechnology, Life Sciences, etc.).
• Ideally 3-5 years of experience in Clinical Quality oversight (clinical QA experience in the pharmaceutical industry required).
• A complete understanding and application of principles, concepts and practices of clinical research procedures is required.
• A high level of English language, both written and spoken.
• A high level of attention to detail.
• The ability to work independently, to prioritize her/his own work as well as to prioritize task and coordinate other team members.
• Excellent interpersonal skills, ability to work in teams, flexibility in changing tasks and priorities and motivation for new challenges.

Location:

We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.