CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "GCP regulations"

Clinical Project Lead

To actively work in collaboration with a cohesive clinical development team that values professionalism, process and results achieved in alignment with applicable SOPS, Working Practices, ICH/GCP and Regulations.

Research Director- 18 yeras if experience managing sites

I have over 18 years of professional experience established in clinical research. As my resume indicates, I have experience in all aspects of clinical trials. I recently worked as the Director of Clinical Operations in a clinical site where I performed all aspects of clinical trials and the daily operation including problem solving. I have successfully managed the quality assurance department and acted as a trainer for t...

Executive Office Assistant

I am currently seeking a position which will allow me to demonstrate my qualities as a responsible and resourceful team player. My knowledge includes extensive experience in the healthcare and clinical research arena, compliance training and analyzing, training coordination, Learning Management System testing and training, process development and implementation management, medical billing processing management, inventory ...

Tags for this Online Resume: Auditing, internal and external, GCP regulations, Writing Processes and Procedures, SOP development, Excel Reports, Inventory

Clinical Research Coordinator New Orleans, LA

Monitor assigned clinical trials, interact with all different department such as (monitoring resources, project manager, quality assurance and data management). Conduct site visits (initiation, monitoring and close out). Ensure the adherence to FDA, ICH & GCP regulations. Instruct the site staff in their roles and responsibilities in conducting clinical trials. Ensure the completion and collection of regulatory document...

Tags for this Online Resume: Clinical Research Coordinator, Data Manager, Medical Assistant

QA

Cover Letter Ignace Vallejo, MS. GCP and GMP QA Manager Certified Quality Auditor GMP; by CFPA. Certified Six Sigma “Black belt”. 525 Neptune Ave, Brooklyn, NY 11224. Apt 22 F Home # 718 946 0556. Mobile # 917 359 3028. ignaciovallejo@optonline.net Good Clinical Practice (GCP). Audits were followed according to our SOPs and ICH GCP regulations and Guidelines. The vendor audits were preformed, as follows: • On Octo...

Tags for this Online Resume: Quality Assurance, Scientist, Trainer, Quality Control, Auditor, Biology, Quality, Manufacturing, Management, Microbiology

Assistant Manager - 10 Years of Experience - Near 07041

Summary of qualifications: * Experience with Evaluating Reports and Creating Statistical sharing Platforms for Pharmaceutical Industry, Hematologic Oncology, Aphaeresis, Bone Marrow Transplantation and Cellular Treatment fields, Orthopedic Surgery, * Pharmaceutical, Furniture and Medical supply industries management and director experiences. * Representation and Building good relationship between industries and Associations...

Tags for this Online Resume: Statistics, Cellular, Oncology, Surgical, Trauma, Networking, Orthopedic, Orthopedics, Pharmaceutical, Wholesale

Quality Assurance Manager / Vendor Manager - 20 Years of Experience - Near 60060

SUMMARY: Experienced, dedicated, Quality Assurance professional and trainer who provides the knowledge and skills to assist with and drive projects as part of a team or as an individual contributor. * 20+ years of experience in pharmaceutical research, 15+ in Quality Assurance * Experience with Good Clinical Practice (GCP) regulations, the International Conference on Harmonization (ICH), Good Laboratory Practice (GLP), Vend...

Tags for this Online Resume: Quality Assurance, Test, Clinical Research, Research, Audit, Management, Pharmaceutical Industry, Development Activities, Policies and Procedures, Vendor Management, Clinical, GCP, GLP, Training, Nonclinical research, Preclinical, Early phase clinical research