Viewing 1 - 10 of 22 jobs
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...
Regulatory Affairs Associate * 510(k),IDE,PMA (original/revision/supplements) preparation, submission and ... and implement strategies and activities required to procure regulatory approval for new and revised product lines.
The Associate, with minimal guidance, prepares, reviews and submits high quality, regulatory submissions to the FDA ... of other FDA submissions. * Evaluates changes to regulatory documents and formulates strategies to maintain...
He/she represents Regulatory Affairs on project teams and serves as team leader for projects ... drugs for the US market. -Development of new Regulatory Affairs Associates into fully contributing staff.
Associate Director of Regulatory Affairs Pharmaceutical Labeling Contract position 6 months to 1 year There is an ... products group recruiting in engineering, quality, regulatory, marketing, and operations in medical devices,...
of the Sr. Manager. With minimal guidance this senior level associate attends and represents Regulatory Affairs at ... Reviews and analyzes regulatory and related publications to assure compliance and anticipate future regulatory action 6...
for at least 3 years experience in post-marketing regulatory affairs, specifically pharmaceutical promotional ... Nearest Major Market: New Jersey Job Segments: Regulatory Affairs, Manager, Hematology, Oncology, Medical...
He/she represents Regulatory Affairs on project teams and serves as team leader for projects ... for generic drugs for the US market. * Development of new Regulatory Affairs Associates into fully contributing...
Commercial business, including support to Infant Formula, Regulatory Affairs, and Operations businesses. Products ... research and development, quality, medical affairs, regulatory review and approving marketing materials and...
and record information according to Novartis and regulatory guidelines - Conduct medical review of ... launch management teams [LMT], Global Oncology Scientific Affairs) - Develop comprehensive compendia strategies for...