Associate Country Clinical Quality Manager

A minimum of 4-6 years of relevant experience in clinical research including direct field monitoring experience or management/oversight of such individuals, with a demonstrated record of accomplishments.

Knowledge and understanding of Clinical Trial processes as well as quality management and control tools is required.

Experience of participating in cross-functional teams of business professionals, Experience of leading a cross-functional team is a plus.

Experience of participating in audits and inspections, preferably with experience of a direct support.

Clinical Quality Management, Clinical Research, Clinical Study Design, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Quality Management, Regulatory Compliance

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Our Company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products.

Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

We are looking for an Associate Country Clinical Quality Manager to support the quality of clinical trials conducted by the Clinical Trials Operations in UK.

It is critical that, for all our sponsored clinical trials, patient safety, high quality data and compliance with company requirements and regulations are delivered and sustained.

Under the guidance of the Director, Country Clinical Quality Management Lead (CCQM-L) and in close collaboration with the Country Clinical Quality Manager (CCQM), the Associate CCQM supports the oversight of specific CQM activities in the respective country/cluster.

In addition, the Associate CCQM supports audits, inspections as well as Quality Control and local training activities.