Global Aggregate Reports and Risk Management Lead
hace 7 días
Job Summary
As a Group Head of Aggregate Reports and Risk Management, you will be responsible for leading a team of Senior Global Risk Management Plan Managers and Senior Medical Writers in the development of robust and feasible Risk Management Plan strategies and Aggregate Reports for assigned high-priority products/therapies. You will ensure that these strategies are aligned with the benefit-risk profile of the products and supported by complex stakeholder matrices.
About the Role
The Group Head, Global Aggregate Reports & Risk Management, will lead a group of Senior Global Risk Management Plan Managers as well as Senior Medical Writers and AR&RM Analysts in the development of robust and feasible Risk Management Plan strategies and Aggregate Reports for assigned high-priority products/therapies, aligned with the benefit-risk profile of the products and supported by complex stakeholder matrices.
Key Responsibilities
Responsible for timely high-quality deliverables either through direct involvement in processes or through assignments taking into consideration individual workload, experience, location, business needs, and individual development needs.
Interacts with GPTs and Functions (e.g., GPH, HPS, Medical Writing, Regulatory Affairs) to ensure proper prioritization of programs and assign adequate resources.
Aligns the support provided by Global (Sr) RMP Managers/(Sr) Medical Writers/AR&RM Analysts to the Global teams in developing and maintaining the Safety RMPs, RMP strategy, and Aggregate Reports with business rules, regulatory guidelines, and company standard operating procedures.
Responsible for recruiting, developing, retaining (Sr) Global RMP Managers/(Sr) Medical Writers/AR&RM Analysts, developing and implementing an onboarding program for new hires.
Provides operational and strategic guidance on RMP & AR processes, policy, templates, and training.
Responsible for AR & RM team objectives according to company and department priorities, development plans, and ongoing feedback on performance of direct reports.
Member of the AR&RM Leadership Team. Collaborates with Global Head Aggregate Reports & Risk Management in setting the department's objectives and achieving them.
Advises and influences the organization regarding Aggregate Reports & Risk Management concepts, strategy, and processes, relevant for product submissions and launches worldwide as well as for lifecycle management by close connection with stakeholders and industry peers.
Guides a cross-functional matrix in the development of tools for RMP preparation, implementation tracking, working practices, and guidelines, implementation of regulatory guidelines, and Safety RMP project management.
Acts as AR&RM Subject Matter Expert (SME) in inspections and audits as, including handling of pre-inspection/audit requests, participating in interviews with inspectors/auditors, and supporting CAPAs.
Acts as AR&RM SME for assigned collaborations at early stages of partnerships, e.g., integrations, mergers, and acquisitions. Influences these collaborations beyond Patient Safety, in global and local cross-functional and cross-divisional aspects of RMP, e.g., Regulatory Affairs, Marketing, Countries, which impact worldwide launches.
Represents AR&RM in MSRB, GLC, GPTs & SMTs and other relevant boards/teams and provides expert opinion as required.
Evaluates the impact and ensures compliance in collaboration with OPEX of worldwide regulations and industry practices on current AR&RM plans strategy, processes, and tools (e.g., ensures the templates and internal guidelines on strategy are in accordance with new/changing regulations). Drives the internal alignment on the company position with multiple functions and boards involved.
Oversees the Global Teams' strategies for AR & RMP related responses to Health Authorities.
In collaboration with OPEX and the AR&RM office, designs, develops, and maintains metrics to monitor quality of RMPs & AR, and escalates to Head of department, QPPV, PS&PV leadership, and cross-functional boards any potential risk and issues.
Provides input into the development of regular and up-to-date AR & RM training to the organization (namely SMT/GPTs, Medical Safety, Regulatory, Quantitative Safety and Epidemiology, Clinical, Medical Affairs).
Deputizes for the Global Head Aggregate Reports & Risk Management e.g., MSRB for AR & RMP related aspects, and strategic initiatives.
Deputizes for other Group head when required supporting their team.
Requirements
Scientific Degree required. Life sciences degree desirable. Advanced degree (Masters, MD, PharmD or PhD) required.
Fluent in spoken and written English.
Why Novartis?
Novartis is a global healthcare leader dedicated to discovering new medicines to improve and extend human life. We believe that the best way to create a healthier world is by putting patients at the center of everything we do. We are committed to using our innovative medicines to improve the lives of millions of people around the world.
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Accessibility and accommodation:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to ****** and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Division: Development
Business Unit: Innovative Medicines
Location: Spain
Site: Barcelona Gran Vía
Company / Legal Entity: ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.
Functional Area: Research & Development
Job Type: Full time
Employment Type: Regular
Shift Work: No
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