Medical Affairs Manager - Parsippany

+Job summary · This role serves as a strategic partner and operational leader within the Medical Affairs organization · +Responsibilities:Lead strategic planning and operational activities across Field Medical Affairs · Provide meeting management support for national MSL team mee ...

This role serves as a strategic partner and operational leader within the Medical Affairs organization, · supporting US field initiatives.Lead strategic planning and operational activities across Field Medical Affairs. · Provides meeting management support for national MSL team m ...

This role serves as a strategic partner and operational leader within the US Medical Affairs Oncology organization, · supporting CCC (Community Cancer Collective) and SEC (Strategic Evidence and Collaborations) initiatives.The position partners with cross-functional teams to driv ...

This role is hybrid in either Parsippany NJ or Foster City CA. This role serves as a strategic partner and operational leader within the Medical Affairs organization supporting US field initiatives. ...

This is a contract opportunity with long-term potential located in Parsippany, NJ OR Foster City, CA (Hybrid). The Senior Manager – Medical Affairs will lead strategic planning and operational execution across US Field Medical Affairs. · ...

+Job summary · Immediate need for a talented Senior Manager – Medical Affairs (US Field Medical Operations) (Virology and/or Oncology). This is a contract opportunity with long-term potential. · +Responsibilities:Lead strategic planning and operational execution across US Field M ...

This role serves as a strategic partner and operational leader within the Medical Affairs organization. · Support US field initiatives. · Drive operational excellence, strategic planning, and project execution to support the US Field Medical Team · ...

You will conduct timely medical and scientific assessments and critically review ingredients, products, technologies, processes, · and competitor products relevant to the brand or category space. · ...

We're building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. · Oversee the strategy, content and continuous improvement of the Corporate Affairs Community Site ensuring it serves as a dynamic hub for knowledg ...

Under general direction, responsible for successfully filing original Abbreviated New Drug Application submissions and for managing post approval changes requiring regulatory submissions. · ...

Under general direction, responsible for successfully filing original New Drug Application submissions and for managing post approval changes requiring regulatory submissions. · ...

Under general direction responsible for successfully filing original Abbreviated New Drug Application submissions and for managing post approval changes requiring regulatory submissions. Can be primary contact with regulatory authorities for assigned projects and products. · ...

+Under general direction, responsible for successfully filing original Abbreviated New Drug Application submissions and for managing post approval changes requiring regulatory submissions. · ...

We are seeking a seasoned Regulatory Project Manager with deep NDA experience to lead and shepherd a New Drug Application (NDA) through submission and approval. · ...

Gilead seeks a Manager to support the U.S. Medical Affairs HIV Treatment Strategy team. · ...

We are seeking a seasoned Regulatory Project Manager with deep NDA experience to lead and shepherd a New Drug Application (NDA) through submission and approval. · Lead end-to-end NDA planning, execution, and submission activities · Drive project timelines, deliverables,and risk m ...

The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.This individual is recognized as a very knowledgeable in their discipline expert and in regulatory affairs sub ...

US Agent for all products responsible for communication between the FDA and manufacturing sites. Communicate and follow-up status with FDA for any Chemistry Bioequivalence and Patents issues. · Lead train and guide the CMC team to ensure highly qualified personnel. · ...

The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.With input from the submission teams, this individual establishes and maintains submission content planners an ...

At Gilead we're creating a healthier world for all people. For more than 35 years we've tackled diseases such as HIV viral hepatitis COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. · ...