Johnson & Johnson is seeking an Associate Director, Cross TA Clinical Risk Management to join our R&D Quality CRM team. The role supports trials and programs across multiple countries, including the United Kingdom.
You will coordinate the identification, assessment, and mitigation of quality risks to protect data integrity and patient safety. You will lead risk reviews, maintain Clinical Quality Plans, drive risk monitoring, and advise on CAPA and inspection readiness.
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Senior Clinical Risk Director, Cross-TA in High Wycombe employer: Johnson & Johnson Innovative Medicine
At Johnson & Johnson Innovative Medicine, we pride ourselves on fostering a collaborative and inclusive work culture that empowers our employees to thrive. As a Regulatory Medical Writer II, you will benefit from our commitment to professional development, with ample opportunities for growth and learning in a dynamic environment. Located in the UK, our hybrid work model offers flexibility while allowing you to contribute to impactful projects that advance healthcare globally.
Contact Details:
Johnson & Johnson Innovative Medicine Recruitment Team