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The Position
Function: PDQ
Department: RBQM CoE
This role reports into the Global Head of RBQM as part of the RBQM Leadership Team
In Pharma Development Quality (PDQ) we strive for confidence in the integrity of our data and our processes, agility, and unrivaled transparency with health authorities, patients and society. Our work provides leadership, know-how and partnering on quality across Molecules (GCP), Products (Drug and/or Medical Devices), Pharma affiliates and global regulated processes
RBQM Head:
Risk Based Quality Management (RBQM) is a proactive risk management approach that directs focus to the areas of greatest operational risk while maintaining quality and compliance and reducing low impact work. RBQM is a system that reduces the errors that matter to the protection of participant safety, the reliability and interpretability of the study data, and the decisions made based on the study results. RBQM helps study teams to design quality and maintain trial oversight through ongoing and continuous surveillance of information, trends and metrics. By building quality and risk management approaches into the scientific design and operational conduct of clinical trials, risks can be mitigated and issues can be detected early on, or prevented entirely.
The RBQM Head plays a critical role in ensuring the success of embedding RBQM at Roche. This senior position is responsible for spearheading the strategic technical & process direction of the RBQM Center of Excellence (CoE) ecosystem; essential for effective RBQM implementation. In this role it will be crucial to ensure alignment between process and people while ensuring the right skills and talent are in place to support the RBQM ecosystem . The ideal candidate blends strong technical/systems knowledge with strategy leadership. They have the ability to strategically lead a team in a fast-paced environment where there is often ambiguity. With the right technical strategies, processes and talent in place, the RBQM Head can ensure that RBQM leads to improved risk management, enhanced quality oversight, and more efficient clinical trial and drug development processes.
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