Clinical Quality Assurance Program Lead (Associate Director)

London - UK

Monthly Salary: Not Disclosed

Posted on: 11 hours ago

Vacancies: 1 Vacancy

Job Summary

Job Description Summary

LOCATION: London UK Dublin Rep of Ireland Barcelona Spain
ROLE TYPE: Hybrid Working #LI-Hybrid

The Associate Director Clinical Quality Assurance (QA) will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements the internal standards and a full adherence to patients safety rights and well-being.

Job Description

Key Responsibilities:

Proactively provide QA leadership to the business strategy for assigned programs/trials by ensuring considerable organization awareness (e.g. Interrelationship of departments and business priorities)
Drive implementation of quality strategy within Global Clinical Team (GCT )/ Clinical Trial Team (CTT) under responsibility
Regularly monitor the implementation of the annual Quality Plan pertaining to the assigned programs/studies
Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that Clinical Trial Process (CTP) are in control
Provide robust and clear quality oversight in the following areas of clinical development:
- Support/collaborate with key stakeholders (e.g. Country Development Quality (CDQ) Development Units (DUs) GCT and/or CTT members) to ensure that risks are detected and remediated.
- Support core governance for quality incident management for critical and major deviations pertinent to the programs being assigned and ensure timely escalation when required.
- Provide Good Clinical Practice (GCP) guidance to day-to-day questions arising from Clinical trials deliverables.
- Collaborate with Country Development QA and External Service Providers (ESP) QA to drive initiatives relevant to internal monitoring and outsourced activities Quality oversight.
- Lead inspections preparation and facilitation in collaboration with other QA groups within Research & Development Quality (RDQ).
- Support audits and inspections follow-up activities including Corrective & preventative Actions (CAPA) preparation.
Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.
Active participation in continuous improvement initiatives (including Work streams) and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability
Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.

Essential Requirements:

Bachelors degree in life science or healthcare field required. Advanced degree or equivalent education/degree in life sciences/healthcare preferred (PhD/MD/ PharmD/ Masters).
7 years of involvement in regulated activities (GCP/ Pharmacovigilance (PV)) clinical development and/or QA positions.
Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product
development.
Ability to work independently and in a global/matrix environment.
3 or more years experience in managing projects.
Strong skills in GCP quality and/or clinical development

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Required Experience:

Director

Job Description SummaryLOCATION: London UK Dublin Rep of Ireland Barcelona Spain ROLE TYPE: Hybrid Working #LI-HybridThe Associate Director Clinical Quality Assurance (QA) will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compli...