Clinical Quality Operations Manager - Remote

Clinical Quality Operations Manager

In partnership with the Clinical Quality Operations Lead and Head of Clinical Quality Operations, the Clinical Quality Operations Manager (CQOM) is accountable for the execution of operational quality activities within the assigned therapeutic area. This includes operational quality management and inspection management activities. The CQOM will oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic area to proactively embed quality into our company's sponsored trials, ensure adequate vendor oversight, and address any quality issues as needed.

The incumbent will be accountable for the development of quality plans to implement `quality by design` within clinical development programs, using a risk-based approach. The incumbent will be accountable for the overall strategy for maintaining ongoing inspection readiness as well as preparing for, managing, and following up on regulatory inspections.

Responsibilities include:

• Overseeing the strategic implementation of `quality by design` principles in assigned clinical trials.
• Developing Risk Assessment and Categorization Tools and Quality Plans in partnership with the Clinical Trial Team (CTT).
• Performing a TA-level review of quality plans and risk mitigation approaches to identify emerging signals or trends and provide relevant feedback.
• Facilitating and overseeing responses to audit and inspection observations.
• Developing skillsets to recognize and respond to new and emerging risks through the use of technology.
• Building and enabling effective working relationships with key stakeholders.
• Contributing to the standardization of Clinical Quality Operations procedures, tools, and templates.
• Ensuring comprehensive oversight of all activities delegated to third parties.
• Maintaining current regulatory inspection knowledge and leading GCP inspections.
• Developing inspection management plans and ensuring cross-functional team preparedness.
• Ensuring timely implementation of actions and commitments related to audits and inspections.
• Providing input into GCP Quality and Compliance Council and strengthening company programs.

Education: B.A./B.S. or M.A./M.S. Degree or equivalent in a relevant health care area. Further formal education in quality management or business management is preferred.

Prerequisites: Minimum of 6 years in clinical research including at least 2 years with developing and managing clinical quality systems and management of regulatory inspections. Profound knowledge and comprehension of clinical development programs, clinical trial processes, quality management systems, and quality control tools. Expert knowledge of GCP/ICH and worldwide Regulatory Health Authority requirements. Has delivered effective CAPA management solutions. Has worked with risk management tools and processes within the clinical quality framework.

Skills: Superior oral and written communication skills in an international environment. Ability to manage and develop others, including formal performance management when necessary. Excellent project management and organizational skills. Excellent teamwork and leadership skills, including conflict resolution expertise and discretion. Ability to lead cross-functional teams of business professionals within and outside our Research division. Able to act urgently for worldwide health authority inspection matters. Ability to analyze, interpret, and solve complex problems. Ability to think strategically and objectively and with creativity and innovation. Ability to proficiently interact with all levels of specialists & management and exert influence to achieve results. Ability to identify and summarize the key issues from audits and inspections and to develop and deliver lessons learned.