International program regulatory director

Job Description SummaryThe International Program Regulatory Director (IPRD) is responsible for providing strategic support and oversight to global and regional teams on the design and execution of optimal registration strategies and plans for the assigned portfolio in the assigned International countries.By partnering efficiently with relevant global DU line functions (LF) and International (INT) cross functional stakeholders, the IPRD drives the process of registration plan design, alignment and sign off with relevant regulatory, commercial and DU stakeholders in global, region and countries in INT markets except for China, Japan and the European Union. The IPRD ensures the timely dissemination of consolidated plans to the relevant global and INT stakeholders. The IPRD uses global, regional and country sources to ensure the maintenance of country requirements, pipeline information and registration plans across all INT markets and their efficient communication to INT stakeholders. They partner with relevant line functions to optimally translate new requirements into tangible NVS plans. IPRD leads and oversees the implementation of initiatives to enhance efficiency in ways of working and functional excellence.The IPRD is member of the global RA subteam and leads the INT RA subteam of assigned countries. They may lead or contribute to regional cross-functional initiatives and committees and may represent International RA in global cross-functional initiatives and committees. The IPRD may act as deputy to the Regulatory Head Pipeline Management, Compliance and Operations. Job DescriptionKey ResponsibilitiesSets up and manages the INT RA subteam comprised of global and country RA roles from countries in scope with the objective of generating optimal registration strategies, ensure their inclusion into global plans and their efficient execution. Represents countries in scope of the INT subteam at the global RA subteam level.Upon notification letter dispatch and for major updates thereafter, the IPRD drives the process of registration plan design, alignment and sign off with relevant regulatory, commercial and DU stakeholders in global, region and countries in all INT markets except for China, Japan and the European Union. Is accountable for the appropriate dissemination of agreed plans to relevant stakeholders in the organization.Oversees the up to date maintenance and execution of registration plans for all INT countries in alignment with RA INT and RA DU, including procurement of ancillary document for submission dossier, review of and contribution to responses to Health Authority (HA) questions, follow up on key milestone activities by relevant RA and LF stakeholders. Maintain up to date contact CO contact lists for programs and COs in scope.In alignment with DU RA and RA transactions team, may provide specific support to integration assets for INT countries. In partnership with DU RA roles (GPRDs, GRTLs), is responsible to generate overviews of pipeline programs and to disseminate them to relevant INT stakeholders to support strategic and operational planning.Partners with global LFs and Regional / country RA roles on regulatory emerging new regulatory policies and requirements and ensures their optimal interpretation and use in project strategies and implementation plans. Is accountable the up to date maintenance of repositories of country requirements and dissemination of information to relevant stakeholders.   IPRD leads and oversees the implementation of initiatives to enhance efficiency in ways of working and functional excellence. Takes a leading role in designing and actioning registration plans for Emerging Markets Brand and acts as main contact point within RA INT for the Emerging Brands Center of Excellence for the portfolio in scope.In alignment with relevant DU, may act as lead RA role on the registration of products that target diseases which are predominantly prevalent in INT countries. Partners with GRSS&C LCM group on geographic expansion plans and execution for INT countries. Partners with RA INT roles and global policy on identification & shaping of policy changes in INT countries.Oversees dissemination of information to and education of global roles on INT country/regional requirements. Support the execution of, or act as a region representative in functional or cross-functional initiatives, particularly those with potential impacts on INT RA resources or FTE allocations.Mentors International Program Regulatory Managers and Sr. Managers on ways of working on pipeline management ensuring compliance with NVS quality standards. In partnership with the operational manager, identify and facilitate growth and development opportunities, supporting a culture of continuous learning.May participate in recruitment of IPRM/D associates and their development. Champion Novartis culture, values and behaviors and demonstrate behaviors in action in-line with Novartis leadership expectations. May act as deputy of RA Head Pipeline Management, Compliance and Operations.Meets objectives as defined in registration plans for the countries and portfolio in scope. Proof of maintenance and communication of country requirements and registration plans for INT countries.Minimum RequirementsMinimum of 8 years in Regulatory, product development, minimum of 2 years country, regional or global RegulatoryProven track record of HA negotiations, ability to develop and communicate strategic visionAbility to work in cross-functional environment, Proven expertise in project managementHighly committed and team oriented, Proven strong leadership skillsProven track record of early recognition of potential regulatory issues, complex situations, sound risk assessment and overcoming hurdlesProven track record of successful risk assessmentAbility to travel and represent the organizationScience based BS or MS with requisite experience and demonstrated capability, advanced degree (e.g., MD, Ph D, Pharm D) preferred.Commitment to Diversity and 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 individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform 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  Skills DesiredClinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution