Serious Breach Office, Sr. Specialist

Johnson & Johnson Johnson & Johnson · Pharma · Beerse, Antwerp, Belgium

This role is a Senior Specialist in the Serious Breach Office (SBO) within the Clinical Risk Management-Operational Excellence (CRM-OpEx) function of R&D Quality (RDQ) at Johnson & Johnson. The primary focus is on ensuring compliance with country and regional serious breach reporting requirements for JJIM sponsored clinical trials. Responsibilities include facilitating assessments and reporting of issues to Health Authorities, monitoring process performance, driving continual improvement, analyzing data for dashboards, and collaborating with various stakeholders including Legal and Regulatory Affairs. The role requires vigilance in regulatory landscape research and managing projects independently.

What you'd actually do

  1. As a facilitator of the serious breach process and record owner, you will drive the assessments and reporting of issues or events related to JJIM clinical trials that meet the serious breach reporting criteria to the appropriate corresponding Health Authorities.
  2. As a designated SBO Lead, you will define, drive and enhance oversight strategies and monitoring capabilities to ensure the effectiveness and compliance elements of the serious breach process within clinical trial risk and issue management framework.
  3. You will develop, assess and report performance metrics related to quality, efficiency, and risk for serious breach process execution and timely case reporting identifying process and/or compliance strengths and gaps for management review.
  4. As a steward of continual process improvement, you will monitor adherence to implemented process controls, effectiveness and risk management requirements in alignment with associated business partner processes, enterprise standards and industry regulations to develop proposals for optimization initiatives.
  5. As a presenter and primary monitor of serious breach reporting process effectiveness, you will collaborate with stakeholders to create and monitor meaningful digital dashboards that enable clear interpretation and data-driven decision making.

Skills

Required

  • Clinical trial quality management
  • Regulatory compliance
  • Process facilitation
  • Data analysis
  • Stakeholder management
  • Project management
  • Communication skills

Nice to have

  • Experience in healthcare or pharmaceutical industry
  • Knowledge of global health authority regulations

What the JD emphasized

  • serious breach reporting requirements
  • serious breach reporting
  • serious breach process