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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..
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 ..
... information May lead ad hoc regulatory safety requests by obtaining data ... development and authorship Leads ad-hoc regulatory safety requests preparation by obtaining ... Departmental Activities Leads preparation for..
Job Information Bristol Myers Squibb Associate Director, Safety Science in Summit New ... information May lead ad hoc regulatory safety requests by obtaining data ... surveillance activities, signal assessment, and..
Job Information Bristol Myers Squibb Associate Director, Product Quality Support Surveillance in New Brunswick New Jersey Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, ..
... 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...
... on internal/external system audits and regulatory agency inspections Responsible for business ... documentation system in compliance with regulatory requirements, company requirements and procedures; ... research, analytical, quality, engineering, manufacturing,..
Job Information Bristol Myers Squibb Associate Director GxP External Engagement in New ... the External Engagement team, the Associate Director, GxP External Engagement plays a ... that BMS is recognized..
... make a difference. Position: Executive Director, Regulatory Affairs Team Leader Supervisor: Vice President, ... Team Leader Supervisor: Vice President, Regulatory Affairs Department: Global Regulatory Affairs Prerequisites Bachelors in scientific..
... and make a difference. POSITION Director, Regulatory Affairs SUPERVISOR Senior or Executive Director, Regulatory Affairs DEPARTMENT Global Regulatory Affairs PREREQUISITES Bachelors in scientific discipline; ... industry experience in in..
... Responsibilities Leadership responsibility for global regulatory strategy within the Hematology portfolio. ... portfolio. Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing ... for indications..
... will you bring? Description The Associate Director, Competitive Intelligence (CI) & Knowledge ... Business Development, Commercial, R&D, Medical Affairs, Market Access, Clinical Research & ... Clinical Research & Development,..
... 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 ... on behalf..
... and make a difference. POSITION Associate Director/Director, WW Medical Affairs Hematology Myeloid SUPERVISOR Senior Director, WW Medical Affairs Hematology Myeloid DEPARTMENT WW Medical ... Hematology Myeloid DEPARTMENT WW Medical..
... difference. Summary: Reporting to the Associate Director, Worldwide Patient Safety (WWPS), Aggregate ... other departments such a Medical Affairs as needed Adhere to the ... content or process to..
Description The Director, Actuarial Analytics/Forecasting analyzes and forecasts ... financial and competitive position. The Director, Actuarial Analytics/Forecasting requires an in-depth ... or segment. Responsibilities As the Director of Part D..
