or Dublin, Ireland Internal Job Title: Global Program Regulatory Director Novartis is seeking a Global Program Regulatory... Director (GPRD) to lead global regulatory strategies for development and marketed products. This role integrates inputs...
and proactive Senior Global Program Regulatory Manager to join our Global Regulatory Affairs team.The role involves directing the... or Dublin, Ireland Internal Job Title: Senior Global Program Regulatory Manager We are looking for an experienced...
Program Regulatory Director (IPRD) in partnering with Development Units (DU) RA roles to obtain, digest and communicate... language. Experience in Regulatory, product development Country, regional or global Regulatory Affairs experience. Proven...
Internal Job Title: International Program Regulatory Director Novartis is seeking an International Program Regulatory... or MS with requisite experience and demonstrated capability. Experience with country, regional or global Regulatory Affairs...
Internal Job Title: International Program Regulatory Manager (IPRM) Are you passionate about driving global regulatory... initiatives—all while working under the guidance of the International Program Regulatory Director. Job Description Key...
Job Description We are recruiting for an exciting role for a Director SPRI EU & EEMEA Regulatory Operations... to be based in either London or Brussels. You will report to the Executive Director, Regional Regulatory Operations Lead, EU...
effective integration of broad regulatory ideas/tactics supporting program strategy. This roles assignments may be global... documents and Health Authority communications Counsels and advises GRA leadership on status of global Regulatory Affairs...
Director will be responsible for the access evidence planning and execution for a program within BioMarin's Enzyme Therapies... Access & Strategic Pricing. It will include a high degree of cross-functional collaboration with medical affairs, regulatory...
and activities within a defined global clinical development program and/or global clinical trial (e.g. clinical development plan.... Leads development of clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures...
with Clinical Operations, Regulatory Affairs, Program Management, CMC, and external CROs to ensure alignment across all trial...Job Description Senior Medical Director, Clinical Development (Oncology) Location: US Remote A global, innovation...
-Functional Collaboration Work closely with Clinical Operations, Regulatory Affairs, Safety, Program Management, and external CRO...Job Description Medical Director, Clinical Development (Oncology) Location: US Remote A global, innovation-driven...
collaboration and decision making for program(s) across (pre/early/full) clinical development and/or medical affairs... organization. May serve as: Global Program Biostatistics Head for a mid to high complexity project and/or Lead Statistician...
Job Description Summary We are seeking a highly motivated Associate Director of Biostatistics... trials/programs within (early/full) clinical development and/or medical affairs. Proven experience in execution and analysis...
Job Description Summary The Clinical Development Medical Director (CDMD) is the Global clinical leader of defined...) and CDP, clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers...
Job Description Summary The Clinical Development Medical Director (CDMD) is the Global clinical leader of defined...) and CDP, clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers...
with cross-functional teams (e.g., business development, external innovation, medical affairs, R&D, regulatory, finance...Title: Senior Director, New Product Strategy & Innovation Company: Ipsen Biopharm Ltd About Ipsen: Ipsen is a mid...
across early- and late-stage clinical development, regulatory strategy, and medical affairs Expertise in key therapeutic areas...Who Are Prescient? We are a specialist, strategic partner to global biopharma companies. We provide expertise...
, Medical Affairs, and the International Commercial organization. In addition, PCO HTA TA Director will represent Novartis...) and aligned with Integrated Evidence Plan (IEP). In partnership with the PCO COE, Global Program Teams, HEOR Leads, HTA Evidence...