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knowledge of statistical methodologies and statistical regulatory requirements. - Previous experience in leading ... methodologies and optimal methodologies acceptable to regulatory agencies. - Up-to-date knowledge of relevant...
client of mine is seeking a Sr.Manager, Regulatory Affairs to join their team in the Philadelphia, PA area. ... Must carry a Master's degree Must have 8 - 10 years of Regulatory Affairs experience within the pharmaceutical...
that range from medical to aviation is seeking a Regulatory Affairs Specialist. The RA Specialist will help plan, ... with the development, implementation and maintenance of regulatory SOP's Participate in continuous (breakthrough)...
by the Manager, Director or Associate VP, Regulatory Affairs. Minimum Requirements: * A Bachelor's Degree ... clinical research experience). 1 to 2 years experience in Regulatory Affairs or Master's in Regulatory Affairs...
of team meetings, representation of Global Regulatory Affairs and provision of regulatory expertise on the ... alignment with Therapeutic Area portfolio, CMC-Regulatory Affairs strategy, commercial strategy, and the Target...
(Years) 5Category Regulatory Affairs - Regulatory AffairsApply for this job:Your application ... Pharmaceuticals USA is looking for a Manager, Regulatory Affairs for our Horsham, PA facility. This...
Sr. Manager, Regulatory Affairs Location: Woodcliff Lake, NJ- Local candidates only please Our growing pharmaceutical ... client is in need of an experienced Regulatory Affairs professional! This is a permanent opportunity to...
As the Regulatory Affairs Project Manager you will provide expertise and leadership for Regulatory projects. You will ... internal resource for information and guidance regarding regulatory issues. The Manager will prepare regulatory...
We are currently seeking a Regulatory Affairs Manager to ensure marketing approval of drug and medical device products ... --Regulatory liason with regulatory agencies and primary regulatory contact for assigned projects. --Supervise...
and product areas as assigned. 3. Liaises with regional regulatory counterparts in the collection and collation of documentation required for international submissions and ensures regional requirements are incorporated into product...