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Online Resumes with "gcp"

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...

Regulatory Affairs Associate, New Jersey

Regulatory Affairs professional with a strong regulatory and compliance foundation, well-versed in the laws, regulations and requirements of the FDA; over six years of experience as an International Coordinator for a pharmaceutical organization, currently completing a graduate degree in Regulatory Affairs in Drug Development, Biologics and Medical Devices, studying all facets of regulatory requirements including processes a...

Clinical Research Professional - Specializing in Study Start Up

I am ready to take my career to the next level. I am a Clinical Research professional specializing in Study Start Up with experoence in: ICFs, Site Regulatory Packages, ICH-GCP, Feasibility and Contract Negotiation.

Tags for this Online Resume: ICH-GCP, Study Start Up, Informed Consent, Contract Site Agreements, Feasibility , Regulatory Documents

Featured Profile

Clinical In-house Monitoring, Clinical Data Management, Central New Jersey

Tags for this Online Resume: Monitor, Data Management, Trial Master FIles, CRF, ICH-GCP, Electronic Data Capture, Clinical In-house Monitor

Project Manager, Clinical Trials

I am interested in a Project Manager or related position requiring multitasking and organizational skills to oversee multiple projects. I have eight years experience in the biotech/pharmaceutical industry. With the scientific, laboratory and management skills I have accrued over the years, I can perform tasks without supervision. I am looking for a position that allows further personal and professional growth.

Tags for this Online Resume: Global Clinical Trials Project Management, ICH, GCP, GLP knowledge, Research Associate , Independent Research , Preclinical trial management, Oncology/Chemotherapeutic drug discovery and development

Clinical Research Manager - RN; 15+ years experience; IRB, GCP, ICH; OHRP, FDA

provide my knowledge and expertise to help further research and compliance with federal research regulations

Tags for this Online Resume: clinical research

Certified Clinical Research Coordinator

To obtain a position as a clinical research coordinator

Ideal Companies: Genentech

Tags for this Online Resume: GCP's, CRF's, Resolve queries, Consent study participants

Regulatory Affairs, Clinical Research, Quality Assurance

A degreed professional with over 4 years of experience in the pharmaceutical/Biotech industry with multi-functional Regulatory, Clinical and Quality background. Demonstrated ability to expand beyond the scope of assigned responsibilities to gain proficiency in new areas. Responsibilities have ranged from managing the preparation, submission of INDs, BLAs, ANDAs/NDA, to reviewing QMS, essential regulatory documents to ensure...

Tags for this Online Resume: Regulatory Affairs, Clinical Research, FDA, GCP, GCP, ICH, GLP, Pharmaceuticals, Quality Assurance

Clinical Research Associate

Highly motivated and experienced biomedical professional with expert knowledge and proficiency in clinical research monitoring. A certified CRA. Hands-on experience in the clinical investigations of novel pharmacological products. Eager to translate expertise gained in research and monitoring to measurable success in the field clinical studies. A demonstrated record of academic achievement and recognition, accompanied by e...

Tags for this Online Resume: Clinical Site Monitoring , Identification and interviewing of potential investigators, ICH GCP Training , Adverse Event Reporting, Study Planning Activities

Regulatory affairs assistant

To work on the assignments in Drug Regulatory Affairs with an organisation of repute preferably in Pharmaceuticals Domain.

Tags for this Online Resume: drug, regulatory affairs, clinical research, GCP, Dossier submission, Pharma industry

Clinical Research Associate, Home Based

I would like to be a member of company where I can establish and grow my career as a Clinical Research Associate.

Tags for this Online Resume: Clinical Research Associate, CRA, FDA, GCP, Regulatory