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Online Resumes with "Clinical Regulatory"
Clinical Regulatory Affairs - 20 Years of Experience - Near 08629
Global Regulatory and Scientific Documentations Intern
Highly motivated and committed individual looking for a career in Regulatory Affairs as well as Research and Development in the pharmaceutical industry. Currently I am working at Bristol-Myers Squibb in the Global Regulatory Department. Works well under pressure in a sustained energetic manner. Comfortable multi tasking in a rapidly changing environment. Given my science education as well as my previous work experience with...
Tags for this Online Resume: Lab Technician , Research , Regulatory , Clinical , Healthcare, Hospital , Pharmaceutical
Clinical Regulatory Affairs - 14 Years of Experience - Near 10552
Clinical Regulatory Affairs - 1 Years of Experience - Near 02134
Clinical Regulatory Affairs - 16 Years of Experience - Near 92116
Tags for this Online Resume: Regulatory Affairs, Clinical Affairs, Compliance, Project Management, Team, Research, FDA
Clinical Regulatory Affairs
Clinical Regulatory Affairs Specialist - 3 Years of Experience
I am seeking to obtain a regulatory affairs position that will allow me to utilize the regulatory affairs skills - learned through education and experience.
Clinical Research - 14 Years of Experience - Near 37601
Tags for this Online Resume: Management , Time and expense report review and approvals, , Home office, Matrix reporting structure , Quality assessments, Budgeting, Successful FDA Audit-Clinical Regulatory Affairs/, Board Member --Treasurer ACRP Chapter in North East Tennessee Region
Clinical Regulatory Affairs - 15 Years of Experience - Near 60564
Clinical Regulatory Affairs - 14 Years of Experience - Near 19053
To obtain a rewarding position in the clinical research field which will broaden organizational, communication, leadership, and collaborative skills and provide an opportunity for further development
Tags for this Online Resume: philadelphia
Clinical Regulatory Affairs - 13 Years of Experience - Near 19711
My background includes 13 years’ experience in the Pharmaceutical Industry at AstraZeneca Pharmaceuticals in Global Regulatory Submissions and Life Cycle Management of Regulatory documents. This includes 6 years’ experience as a Project Manager for Regulatory Global submissions. As a Project manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submiss...
Tags for this Online Resume: Newark, DE, Life Cycle Management, Regulatory Global Submissions, Pharmaceutical Industry, RSS Application, eCTD Publisher, electronic submissions, Regulatory Publisher, Management, Cardiovascular, Document Management, Legal, Pharmaceutical, Project Management, Publishing, Quality Assurance
