Job ID: REQ-10011542Aug 29, 2024SpainSummary: Monitors and audits the company's drug, biologics, or medical devices surveillance program including the intake, evaluation, processing, and follow-up on adverse reports.
Participates in the resolution of any legal liability and in complying with government regulations.
Ensures accurate receipt, maintenance, and assessment against product labeling.
Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports.
May provide trending and safety signal detection and assessment.
Supports all clinical trial activity and post-marketing.About the Role: The Group Head, Global Aggregate Reports Risk Management, leads a group of Senior Global Risk Management Plan Managers as well as Senior Medical Writers and ARRM 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 matrixes.Your Key Responsibilities Include: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/ARRM Analysts to the Global teams in developing and maintaining the Safety RMPs, RMP strategy, and Aggregate Reports with business rules, regulatory guidance, and company standard operating procedures.Responsible for recruiting, developing, retaining (Sr) Global RMP Managers/(Sr) Medical Writers/ARRM Analysts, and 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 ARRM Leadership Team.
Collaborates with the 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 guidance, and Safety RMP project management.
#J-18808-Ljbffr