Director, Global Medical Risk Management
il y a 4 semaines
**Site Name**: Upper Providence, Belgium-Wavre, UK - London, Wavre
**Posted Date**: Mar 16 2023
Sitting within the Office of the Chief Medical Officer (OCMO), the Global Medical Risk Management (GMRM) team partners with the Global Medical (GM) Leadership team, including Medical Affairs, Value Evidence and Outcomes and other functions within the Office of the Chief Medical Officer to create a culture of openness and transparency where staff speak up and leaders take action. GMRM proactively monitors signals and business performance to drive continuous improvement and improve the quality of our decision making across central, regional and local operating company functions. GMRM partners with the business to identify and manage risks in GM which individually, or collectively, influence the achievement of our strategic goals and could jeopardize our license to operate.
As Director, GM Risk Management you will be responsible for enhancing risk management and compliance across our organization and embedding all elements of the Internal Control Framework (ICF). In this highly visible role, you will work with GM Line Leaders, at the Central, Regional and Country level, and other senior staff such as Global Process Owners within the GM business line to identify and manage the Internal Control Framework including risks associated with their business and to understand the current level of control within their business activities. Additionally, you will develop and execute processes within specific GM lines with a focus on ICF maturity and robust risk management.
This role will provide You the opportunity to lead key activities and support assigned GM stakeholder groups at the Central, Regional and Country level, these responsibilities including:
Partner with GM Line Leaders, Global Process Owners and other GMRM associates to understand and enhance the quality and risk management culture, so people at all levels of the organization raise concerns when risks or issues occur, allowing leaders to prioritize key risks impacting business objectives/compliance and address them through early mitigation.
Act as first line of support to assist GM functions to navigate and embed responsibilities relating to policies, SOPs and guidance related to their specific business area as well as address concerns, questions, or issues relating to Global and R&D policies and applicable written standards.
Integrate GSK and R&D risk management written standards and the Internal Control Framework into the GM business processes and ways of working. Onboard and train new senior GM staff (GM LT & LT-1) on the ICF and R&D risk management.
Provide leadership in driving GM objectives relating to managing risks, ensuring that GM’s ‘requirements, needs and interests’ are delivered.
Drive efficient GM strategies for management monitoring performance and facilitating management monitoring need to support Enterprise Risk Management.
Integrate GSK and R&D risk management written standards and programs into the GM business processes and ways of working. Embed GSK enterprise approach to risk and quality management within GM Lines.
Provide leadership in driving GM objectives relating to risk management, ensuring that GM’s ‘requirements, needs and interests’ are delivered and facilitate escalation to the GM Risk Management and Compliance Board or appropriate Enterprise Risk Council.
Support GM Stakeholders through regulatory authority inspections and internal audits.
Maintain contemporary knowledge in the evolving regulatory expectations and global environment that impact the business to proactively manage risks and increase the robustness of our business processes and decision making. Potential to manage GMRM staff in line with GSK’s management expectations; staff may be at an equivalent or lower grade.
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
- Masters degree in Pharmacy, Chemistry, Bio Engineering, Biology, or medical Sciences.
- Proficiency in essential regulation guidelines and Risk Management practices and procedures applicable to R.&D.
- A broad scientific/pharmaceutical industry background in research & development, medical affairs or governance activities.
- Scientific background with more than 8 years of experience in medical affairs and/or clinical research preferably in a related therapy area such as Oncology, Vaccines or Specialty.
- Experience in compliance / risk management type activities.
- Experience of managing and driving complex transversal projects involving senior management.
- Previous experience to implement change management projects.
- Previous line management or matrix team experience is essential.
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
- Experienced in problem solving and issue resolution.
- High degree of communication and influencing skills.
- Excellent leadership skills, promote
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