About this opportunity
Johnson & Johnson Innovative Medicine lists this Manager, Clinical Risk Management opportunity in raritan, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Role: Manager, Cross Therapeutic Area Clinical Risk Management, supporting R&D Quality CRM at Johnson & Johnson
Responsibilities:
collaborate with trial/program teams to identify, assess, and mitigate quality risks impacting trial data, patient safety, and compliance; lead risk reviews, maintain Clinical Quality Plans, support inspection readiness, and guide investigations and CAPA development.
Qualifications:
Bachelor’s degree in a scientific or medical discipline; 8+ years in healthcare/pharma/clinical trials; strong GCP quality and clinical trial experience; excellent communication and cross-functional collaboration skills.
HighValue: focus on clinical risk management within innovative medicine, with familiarity in GxP, ICH guidelines, and inspection preparedness; experience with data analytics tools (e.g., Tableau, Spotfire) and knowledge of GMP, GLP, PV practices preferred.
Work setup: based in Spring House, PA; Titusville, NJ; Raritan, NJ; or international locations (Belgium, Switzerland); up to 10% travel, mostly domestic.
The role involves ensuring trial quality, compliance, and inspection readiness across multiple therapeutic areas and phases, emphasizing risk mitigation and regulatory adherence.
#J-18808-Ljbffr
Worksite address
raritan, NJ, 08869, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.