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Clinical Regulatory Affairs Online Resumes
Medical Affairs, Regulatory Affairs Associate, Clinical Affairs
Doctor of Medicine recognized with clinical trial expertise in medical device, drug safety, regulatory affairs, and post-market monitoring. Strong emphasis on utilization of cross-functional skills to advance medical systems and develop process improvements. Results-driven collaborator with effective oral and written communication and presentation skills. Patient advocate and contributor to public health awareness and educa...
Tags for this Online Resume: FDA MedWatch 21 CFR 820 803, Medical Device Class III, ICD, VT / VF, Medical Affairs, Regulatory Affairs, Drug Safety, Quality Assurance and Management, Public Health, Patient Relations, Medical Communication, SAP, Excel
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 19 Years of Experience - Near 80004
Clinical Regulatory Affairs - 20 Years of Experience - Near 15217
Tags for this Online Resume: oncology, protocol, pharmaceutical, SAEs
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 5 Years of Experience
Seeking an assignment in a globally competitive environment that exposes me to various functions of a assigned work, helps to achieve overall organizational goal, and utilize my past experiences to its best to exceed customer expectations.
Tags for this Online Resume: Filing, Documentation, Focus, Management, Manufacturing, Microsoft Office, Product Development, Project Management, Protocol, Query
Clinical Regulatory Affairs - 10 Years of Experience - Near 92831
Tags for this Online Resume: Research, Billing, Imaging, Accounting, CCS, Compliance, Computer Telephony Integration (CTI), Publications, White Papers
Clinical Regulatory Affairs
Tags for this Online Resume: Pharmaceutical, Clinical Research, Research, Regulatory Affairs, Bilingual, Business Development, Communication Skills, Compliance
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs
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
