Cross-TA Clinical Risk Manager

Johnson & Johnson Co.; Beerse; On-site; EUR 80,000 - 138,000; Full time

Job summary

Johnson & Johnson is seeking a Manager, Cross Therapeutic Area Clinical Risk Management to join our R&D Quality CRM team, coordinating risk identification, assessment, and mitigation across trials and programs to protect data integrity and patient safety.

You will drive risk monitoring, CAPA, and inspection readiness, collaborating with trial teams and governance bodies while traveling up to 10% and maintaining English fluency.

Qualifications

• A minimum of a Bachelor’s degree (scientific, medical, or related discipline).
• A minimum of 8 years working in the healthcare industry (pharmaceutical industry, CRO, or healthcare/hospital system).
• Proven strong GCP quality and/or clinical trials experience.
• Excellent interpersonal, oral, and written communication skills for cross-functional teamwork.
• Flexibility to respond to changing business needs.
• Demonstrated ability to operate in a multicultural environment.
• Proficiency in Microsoft Office applications.

Responsibilities

• Actively participates in study activities, helping identify and mitigate key risks.
• Leads regular risk reviews with risk owners to assess mitigations.
• Maintains Clinical Quality Plans to support risk and mitigation reviews.
• Drives risk monitoring reviews and coaches others on risk mitigation.
• Communicates risk updates to R&D colleagues and governance fora.
• Develops consistent interpretation of issues requiring quality investigations.

Skills

GCP Quality

Clinical Trials

Risk Management

Cross-functional Collaboration

Project Management

Education

Bachelor's degree in life sciences

Tools

Tableau

Job description

Johnson & Johnson is seeking a Manager, Cross Therapeutic Area Clinical Risk Management to join our R&D Quality CRM team, coordinating risk identification, assessment, and mitigation across trials and programs to protect data integrity and patient safety.

You will drive risk monitoring, CAPA, and inspection readiness, collaborating with trial teams and governance bodies while traveling up to 10% and maintaining English fluency.