THE LARGEST COLLECTION OF PHARMACEUTICAL JOBS ON EARTH
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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..
... 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,..
... 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...
... www.astellas.com Astellas is announcing a(n) Associate Director, Project Management opportunity in Northbrook, ... model. Essential Job Responsibilities: Medical Affairs Leadership Lead, create, drive and ... with the GPSTs co-leads..
... Serves as a recognized Medical Affairs authority by maintaining and communicating ... shifts in the external medical affairs environment to predict and maximize ... and accountability with the Medical..
... 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..
... and Scope: The Companion Diagnostic Director, Medical Affairs US, is accountable for the ... diagnostic assay. The Companion Diagnostic Director is responsible for: development and ... with peer leaders..
ROLE SUMMARYrnrnVaccines is the only place in Pfizer where you can contribute to patients in a way like no other – you can prevent sickness and disease. This is at the ..
... our patients. The BBU integrates commercial, market access, medical, digital, and ... to drive scientific development and commercial excellence in the core areas ... and Responsibilities: u003c/bu003eu003cbru003eu003cbru003eReporting to the..
Vir Biotechnology is a commercial-stage immunology company focused on combining ... Duties also include ensuring all regulatory milestones are met, as well ... as maintaining adequate clinical and/or commercial supply..
... Product Quality Lead (Principal PQL), Associate Director of Global Product Quality. The ... through commercialization readiness activities including commercial filing and approvals as well ... Quality management of clinical..
... impact on patientsu2019 lives. SummaryThe Associate Director/Director reports directly to the Head ... handled in accordance with global/local regulatory requirements and company policiesResponsible for ... advisor to Clinical Operations,..
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 ..
... development and successful execution of regulatory strategies, plans and processes for ... new indications / formulations of commercial products and/or life cycle management ... and/or life cycle management of..
The Program Director provides leadership and facilitates others ... (s) Research Agenda. The Program Director provides organization, tracking, budgetary rigor, ... and regional scope. The Program Director enforces governance and..
... 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..
... apply. Purpose and Scope: The Assistant/Associate Director, Oncology Marketing, Health Care Provider ... Sales, Sales Training, Market Research, Regulatory, Health Systems, Legal, Medical Affairs, Global Brand Team, and agencies...
... 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..
... 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/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..
Associate Director, Regulatory Affairs (client dedicated) The Associate Director, Regulatory Affairs will be fully dedicated to ... belong. nn Job responsibilities: This Regulatory position will be responsible for ... will..
