MSD Associate Director Qualified Person 

United Kingdom, England, London 

129037130

Job Description

Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards.

We offer in-depth onboarding and training support to fully integrate our new QP into the role within our Global Development Quality team, setting you up for success in your new role.

This role is based at our Central London office with hybrid working available.

Qualifications and Experience:

• Eligible to be named as a Qualified Person (QP) and to have maintained Continued Professional Development CPD
• Extensive experience in a cGMP environment, preferably gained in a Quality function with respect to clinical trials/IMP environment
• Experience with conducting audits and hosting inspections
• Dynamic individual with excellent organizational skills, who can work effectively and proactively on global functional teams
• Effective verbal and written communication skills in collaborating to colleagues and associates both inside and outside the organization

Closing date for application:05/02/2025

Current Contingent Workers apply

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