Rapidly growing pharmaceutical company is seeking an Associate Director of Regulatory Affairs for its Long Island headquarters.
Candidate will have responsibility to guide and supervise the regulatory team in India with hands-on experience in writing and filing high quality DMF's and their updates conforming to International Regulatory guidelines and authorities expectations.
Over 100 career opportunities now available in the PHARMACEUTICAL INDUSTRY -- multiple locations throughout the United States!
TUSCANY ENTERPRISES IS BASED IN THE SACRAMENTO, CA REGION. WE PARTNER WITH EMPLOYERS NATIONWIDE AND ALSO HAVE MULTIPLE OPPORTUNITIES AVAILABLE THROUGHOUT THE UNITED STATES THROUGH OUR AFFILIATE OFFICES.
Please visit our website at www ...
Seeking experienced Medical Director with proven success in leading clinical development activities for therapeutics targeting Neurological disorders.
*** Attends scientific meetings and fosters and develops strong relationships with investigators.
*** Contributes medical expertise to the development of clinical trials.
*** Assists with the development and implementation ...
Seeking extensive experience in Clinical Development of Alzheimer's Treatments to manage small groups of Medical and Scientific Directors.
*** Supervise the activities of 2 to 5 Medical and Scientific Directors in the Alzheimer's therapeutic drug area.
*** Lead the design and execution of high-level clinical development programs and strategic product development plans.
This is a temporary to permanent employment opportunity as a Regulatory Affairs Specialist.
DUTIES – RESPONSIBILITIES:
The major functions to be performed in this position are as follows:
Participating in day-to-day Regulatory Operations activities with a large emphasis on the development and implementation of systems and procedures used to support regulatory submission activities.
May 26 -
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