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Science & Biotech Online Resumes

Clinical Regulatory Affairs - 12 Years of Experience - Near 55433

I am a medical professional with more than 12 years experience in manufacturing,operation, quality control, research and development and process improvement. I currently seeking opportunities in regulatory affairs.

Clinical Regulatory Affairs - 2 Years of Experience - Near 91377

Clinical Regulatory Affairs

Clinical Operations & Medical Executive with over 25 years years experience overseeing the strategic direction of pharmaceutical, biomedical, and medical device production

Seeking a challenging career opportunity that could maximize my background and expertise in Pharmaceutical or medical device industries as executive overseeing the product developments leading the the clinical operations, medical affairs, regulatory affairs/quality assurance, manufacture as well as overall strategic planing and executions.

Tags for this Online Resume: Clinical Research and Medical affairs, Pharmaceutical and Medicals and device, Senior Vice President or Executive VP or CMO, All locations of the United States and even international, CRO , Chief Medical Officer or Senior Medical Director

Clinical Regulatory Affairs

Clinical Regulatory Affairs

Senior Clinical & Regulatory Dtr./VP with over 20 years experience in all phases of product development.

Over 20 years of experience working in industry in biopharmaceuticals, and Class II-III medical device development. Perform hands-on management of Clinical Operations, and Regulatory Affairs. Oversee cross-functional product development teams and implement systematic project management techniques for clinical trials to ensure alignment with overall product development timelines and market release. Instill continuous quali...

Tags for this Online Resume: clinical research, project management, regualtory, medical device, cllinical trials operations, clinical development, research, IDE, 510(k), CE, PMA, BLA, NDA

Executive Pharmaceutical Sales Professional

Tags for this Online Resume: Pharmaceutical, Medical device

Regulatory Affairs Professional

I'm a clinical regulatory affairs professional with experience in taking medical device products to market in different countries. My experience includes all phases, including study design, budgeting and timeline development, medical writing (e.g., clinical protocol, IND, IDE, etc), clinical study initiation and oversight, data management, premarket notifications (e.g., 510(k), BLA, etc), clinical study reports, and direct ...

Tags for this Online Resume: FDA, ISO, submissions, 510(k), BLA, regulatory strategy, medical writing, management, medical devices

Clinical Regulatory Affairs - 4 Years of Experience - Near 75065

Senior Associate Research Operations - 6 years Industry experience

I am a Life science professional with over 6 years of experience with data mining, interpretation/ writing and document formatting to regulatory guidelines and showcased timely completion of projects with cross functional teams.

Tags for this Online Resume: San Francisco, Clinical trial data management, non-clinical data management, competitive intelligence, Documentation, medical writing

Clinical Regulatory Affairs