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Online Resumes with "Clinical Trial Expertise"
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
Director of Project Management / Clinical Operations, Pharmaceuticals
Pharmaceutical executive with diversified experience in Project and Clinical Trial Management. Proven leadership in the development and implementation of Integrated Development Plans and Life Cycle Planning from discovery to post marketing for Prescription and Over the Counter (OTC) products and in managing complex Phase 1 – 3b Clinical Trials. Expertise in developing and shaping project management groups within an existing...
Clinical In-house Monitoring - 17 Years of Experience - Near 08844
10+ years of proficient experience into clinical research as a Clinical research associate in pharmaceutical industries and clinical research organizations. * In-house and regional monitoring experience in Phase I, II, & III. * Capable to work as both in-house CRA and as a Regional CRA with efficiency to monitor and manage any number of sites depending on Sponsor's SOP. * Good working knowledge of GCP and ICH guidelines. (...
Tags for this Online Resume: Research, Clinical Research, Management, Quality, Quality Assurance, Quality Control, Audit, Oracle, Filing, Good Clinical Practices
