Job Description:This position is responsible for the writing and revision of regulatory documents required for CMC components of INDs and IMPDs, as well as all documents needed for marketing applications (eCTDs). In this key role, the writer will collaborate with CMC technical experts and regulatory affairs to ensure documents are written/revised and submitted to regulatory agencies to ...
Seeking experienced Regulatory Affairs Lead to join a leading biopharmaceutical company with multiple potential blockbuster products in Clinical Trials.
*** Develop and implement regulatory development plans for drug products.
*** Act as point of contact with external regulatory authorities, agencies, investors, analysts, etc.
*** Ensure regulatory strategies and submissions ...
Medical Science Liaison/AD, Medical Science Liaison -CV/Met (San Antonio, TX, OK, AR). Medical Science Liaison will leverage their scientific background,...
Jul 7 - United States
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