GLOBAL RISK MANAGEMENT PLAN MANAGER

Summary Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs.
Participates in the resolution of any legal liability and complying with governmental regulations.
Provides and contributes trending and safety signal detection and risk management assessment for the products’ life cycle.
Provides safety support to the clinical development teams.
About the Role The Global Risk Management Plan Manager Provide support to the medical safety physicians in the management, coordination, development, reviewing, and tracking of Safety Risk Management Plans to ensure that documents are of high quality, regulatory compliant, and that logistics and distribution are handled in an appropriate and timely manner.
Initiates the tracking of commitments and liaises with relevant functions that maintain and monitor the commitments.
Support the Global Product Safety Leader (GPSL) and the designated medical writer for the timely preparation, development and finalization of high quality and regulatory compliant safety Risk Management Plans (RMP).
Support the GPSL/GPT to resolve issues as they arise regarding the RMP strategy, RMP preparation, RMP implementation and RMP overall process.
Guide the GPSL and key authors to ensure that commitments are appropriately worded and reviewed by all relevant line functions and comments incorporated into final document.
Coordinate activities from the different line units to ensure all documents required to support the RMP main document are included in the RMP annexes and available in the Document Management System according to Novartis processes.
Manage all logistical aspects related to the timely development of the safety RMP annexes and works with authors of the different line functions to ensure RMP annexes content meets Novartis and Health Authorities (HA) requirements.
Support the Safety Lead in updating the RMP according to HA requirements and ensures they are aligned with Periodic Safety Update Report (PSUR)/ Periodic Benefit Risk Evaluation Report (PBRER).
Review the RMP to ensure consistency and regulatory compliance of RMP sections and annexes.
Track HA feedback and assessment on RMP and ensures HA requirements are implemented as required (e.
.
in individual RMP, in global RMP template).
Timely submission and delivery of high quality RMPs to Health Authorities.
RMP document and annexes are fully compliant with Novartis and Health Authorities technical and format requirement.
All documents required to support the RMP main document are included in the RMP annexes and available in the Document Management System according to Novartis processes.
Distribution of RMP CoSTA commitments to affiliates and HQ GPT is performed within 15 working days of Health Authority approval.
Database of Health Authorities feedback on RMP is kept up to date.
Experience/Professional requirement.
At least 5 years in a pharmaceutical company, preferably in drug safety, clinical research, or regulatory affairs.
Proven ability to work with large cross-functional teams in complex projects.
Has demonstrated teamwork and effective communication skills.
Works effectively and is able to establish relation- ships with other line functions.
Knowledge in worldwide regulatory requirements for drug registration (scientific and technical aspects) and clinical drug development.
Proven ability to interpret, discuss efficacy and safety data relating to multiple therapeutic area.
Solid Medical/Scientific writing and verbal skills.
Languages.
Fluent in spoken and written English.
Understanding in another major language (e.
.
French, German, Spanish) desirable.
Education (minimum/desirable).
Scientific Degree required.
Advanced degree (Masters, PharmD or PhD) desirable.