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Online Resumes with "Clinical Regulatory"
Clinical Regional Monitoring
Therapeutic experience in IVD Oncology Hematology Orthopedics GI Cardiology Melanoma ENT Multiple Sclerosis and ADHD Extensive knowledge of FDA regulations ICH guidelines GLPs GCPs and SOPs * Monitoring experience of national and international sites for PSSVs SIVs IMVs and COVs * Ability to identify issues and resolve appropriately * Experience multiple EDC systems and platforms
Tags for this Online Resume: Accounting, Policies and Procedures, Project Management, Project Manager, Protocol, Documentation, Cardiology, Clinical Research, Orthopedics, Research
Director - 20 Years of Experience - Near 07039
SUMMARY Medical scientific and marketing communications professional who creates value for pharmaceutical organizations, healthcare providers, and consumers through targeted education for various disease states, product/treatment options, and clinical guidelines. Most recently, I have passionately worked on minimizing patients' exposure to opioids through numerous channels to impact Healthcare Providers (HCP) awareness and ...
Tags for this Online Resume: Business Development, Management, Communications, Professional Services, Services, Consulting, Needs Assessment, Pain Management, Surgical, Sales
Clinical Regulatory Affairs
Graduate of Pharmaceutical Sciences (MSc)
A socially active individual, who is recently graduated from Copenhagen University with grade - 10/A. Practical experience and international studies have given the essential tools to understand complex processes of pharmaceutical industry value chain including drug discovery, regulations, and product commercialization. My calm and flexible personality was proven to be a fit for dynamic working environments as well as workin...
Tags for this Online Resume: Bacterial Transformation, Electrophoresis, clinical, oncology, Communication, Research, Project management, Customer service, Inteligence, Teamwork, Supply chain, protocol, pharmaceutical
Clinical Regulatory Affairs - 20 Years of Experience - Near 94404
Tags for this Online Resume: SAN (Storage Area Network), Management, Product Development, Research, Documentation, Pulmonary, Business Development, Distribution, Pharmacology, Audit
Clinical Regulatory Affairs - 20 Years of Experience - Near 07054
Tags for this Online Resume: Its, Management, Risk Management, Leadership, Planning, Publications, Medical, Documentation, Microsoft Excel, Microsoft Internet Explorer
Regulatory Affairs Specialist - 16 Years of Experience - Near 19464
An accomplished records and information management specialist with proven skill set including 16 years’ experience within records retention and information management. Focus on health authority audit preparedness, compliance, security, and lifecycle management requirements of key company proprietary media encompassing all GXP documentation. Actively liaise with internal areas and external groups including CMOs and CROs to ...
Tags for this Online Resume: Filing, Management, Quality, Quality Assurance, Quality Control, Retention, Document Management, Documentation, Information Technology, Records and Information Management, Regulatory, Operations, Record Coordinator, Compliance, Regulatory Operations
Clinical Regulatory Affairs - 1 Years of Experience - Near 02215
PROFESSIONAL SUMMARY I am seeking challenging and interesting opportunities in the areas of Regulatory Affairs, Quality Assurance, Drug Safety and Clinical Research. I possess strong written and communication skills with minute attention to detail. I am a dedicated team leader who can be relied upon to help achieve targets.
Tags for this Online Resume: Medical, Adobe, Clinical Research, Data Entry, Documentation, ICH, Integrated Development Environments, ISO, Microsoft, Microsoft Excel, clinical, protocol, pharmaceutical, trial, phase
Clinical Regulatory Affairs - 2 Years of Experience - Near 02215
PROFESSIONAL SUMMARY: A Regulatory Project Manager with 2+ years of managing IND/NDA/BLA review processes and 1+ years of cGMPs experience in pharmaceutical industry. Deadline-driven and highly reliable professional, successfully managing over 300 applicants' submissions in IND, NDA, BLA, and BSE as well as participating in 4 cGMPs sponsors' inspections (Japan and Taiwan) and 1 FDA inspection at manufacturing plants. Great ...
Tags for this Online Resume: Compliance, Pharmaceutical, Project Management, Regulatory affairs, CMC, NDA, IND, BLA, cGMP, GCP, ICH
Clinical Regulatory Affairs - 6 Years of Experience - Near 27712
Tags for this Online Resume: Management, ArcGIS, Clinical Research, Communication Skills, Custody, Family Law, Geographic Information System, Litigation, Microsoft, Microsoft Access
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 1 Years of Experience
Tags for this Online Resume: Adobe Acrobat, Documentation, Good Clinical Practices, Regualtory Affairs, Clinical Trials, Clinical Research Coordinator, Regulatory Affairs Associate
