Regulatory Affairs Leader Jobs in Edison, NJ

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Executive Director - Clinical Development Strategy - Medical Affairs  

Novo Nordisk - Plainsboro Township, NJ 08536

to ensure success in the US and Canada. The leader will serve as a leadership team member in the Medical Affairs department. The leader will work closely with other functional department leaders across Global

from: Pharmadiversityjobboard.com - 4 days ago

Director Clinical Operations  

Johnson & Johnson - New Brunswick, NJ, United States

of new systems and tools for clinical operations. Primary Responsibilities : In close collaboration with Clinical Affairs Leaders, identifies and ensures global clinical strategies, resources

from: linkedin.com (+1 source) - 20 days ago

Senior Director, Field Medical Affairs  

Apsida Life Science - Princeton, NJ, United States

stakeholders in the hematology-oncology community. Collaborate closely with cross-functional teams, including Clinical Development, Commercial, Regulatory, and Medical Affairs, to drive the success

from: linkedin.com - 15 days ago

Senior Manager- Technical Product Manager Regulatory Strategy  

Johnson and Johnson - Raritan, NJ

Manager, TPM will partner closely with regulatory affairs leaders to document business processes, optimize these processes, and establish efficient and innovative new approaches for the business. S/he

from: Johnson and Johnson - 2 days ago

Chief Medical Officer - Gene Therapy and Rare Disease  

i-Pharm Consulting - Trenton, NJ, United States

for the next 2 years, they are now seeking an exceptional physician leader to serve as Chief Medical Officer and build out their full R&D function including clinical development, clinical operations, regulatory

from: linkedin.com - 20 days ago

Sr. Director, Global Program Leader  

Genmab - Princeton, New Jersey

, Commercial, Regulatory, and Medical Affairs leaders on the CDT to problem solve and drive key workstreams balancing risk acceptability and expeditious delivery Direct and redirect cross-functional efforts

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from: resume-library.com - 13 days ago

Senior Medical Director  

Genmab - Princeton, New Jersey

of regulatory submissions, safety documents) produced by CDT Act as medical expert and leader in interactions with external stakeholders (e.g., regulatory authorities, KOLs, advisory boards, patient advocacy

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from: resume-library.com - 13 days ago

Global Regulatory Data Manager  

Daiichi Sankyo, Inc. - Bernards, NJ

performance/adherence. As a result, this role will need to partner closely with teams and senior leaders from across Regulatory Affairs, as well as cross-functional stakeholders (e.g., RA CMC, R&D Excellence

from: Pharmadiversityjobboard.com - 24 days ago

Medical Director  

Genmab - Princeton, New Jersey

components of regulatory submissions, safety related documents) Act as medical expert and have the ability to lead interactions with external stakeholders (e.g. regulatory authorities, key opinion leaders

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from: resume-library.com - 22 days ago

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Medical/Scientific Director, Medical Affairs- Psychiatry Pipeline  

AbbVie - Florham Park, New Jersey

to ensure alignment of medical affairs strategies with overall business objectives. Provide medical and scientific support to internal and external stakeholders, including key opinion leaders, clinicians

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from: resume-library.com - 23 days ago


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