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... the development of the CMC regulatory strategy for submissions. These submissions ... IND/CTA, NDA, CTD and MAA regulatory filings. Collaborate with other relevant ... health authorities. Responsible for the..
... with other business processes and regulatory requirements for inspection readiness. Specifically, ... accountable for compliance with key regulatory and quality requirements pertaining to ... the business capability, including system/technology,..
... flows: Change Management (Development & Commercial), Investigations, Action Management, Audits & ... on internal/external system audits and regulatory agency inspections Responsible for business ... research, analytical, quality, engineering, manufacturing,..
... will you bring? Description The Associate Director, Competitive Intelligence (CI) & Knowledge ... and teams in Business Development, Commercial, R&D, Medical Affairs, Market Access, Clinical Research & ... Clinical..
... transformative business results. Summary/Scope: The Associate Director will report to the US ... report to the US Medical Affairs (USMA) Director, Myeloid Data Strategy Lead. He/she ... teams, US..
... innovation and transformative business results. Director, Hematology-Oncology Payer Marketing: Myeloma Job ... are not limited to: This Director role will lead the overall ... Management, Brand Marketing, and Corporate..
... Job Title Senior Manager / Associate Director, PV & Lifecycle Management Quality ... the R&D, GDD, GPS and GMA/Commercial organizations. The RDQ - PV ... Position Summary / Objective..
... and transformative business results. POSITION Associate Scientific Director/ Scientific Director Multiple Myeloma, Global Medical Affairs SUPERVISOR Sr Director, Global Medical Affairs DEPARTMENT Global Medical Affairs PREREQUISITES Advanced degree in..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
... accountability as the WW Medical Associate Director for Immuno-Oncology (I-O), supporting the ... the Markets, with Clinical Research, Regulatory, Commercial, Access, Health Outcomes, Publications, and ... industry experience in..
... are not limited to: This Director (D8) role will lead the ... Management, Brand Marketing, and Corporate Affairs Develop, recruit, and retain the ... funding economics associated with Medicare,..
The Regeneron Associate Director, GVP Quality Management Lead (QML) ... Regeneron global pharmacovigilance (PV) system.The Associate Director will utilize advanced interpersonal and ... in conjunction with business and Director, GVP..
... a difference. The role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply ... apply complex scientific and expert regulatory advice and risk assessment for..
... and transformative business results. POSITION Associate Director / Director of Hematology (Myeloid) Patient Advocacy ... (Myeloid) Patient Advocacy DEPARTMENT Medical Affairs - Patient Advocacy PREREQUISITES This ... with market..
... transformative business results. Summary: The Associate Director, Global Risk Management Strategy reports ... Strategy reports to the Executive Director, Global Risk Management Strategy and ... Plans and/or REMS programs...
... will have accountability as the Associate Director, WW Medical Oncology Melanoma, supporting ... Melanoma team, reporting to the Director, WW Medical Oncology Melanoma. He/she ... the Markets with Clinical..
... Advise and support local Global Regulatory Sciences (GRS) for assessing regulatory landscape and regulations to optimize ... and regulations to optimize our regulatory strategies and submission plans within .....
... transformative business results. Summary The Associate Director will assume leadership responsibility for ... assume leadership responsibility for global regulatory strategy within a development team ... indications that are at..
