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Online Resumes with "GCP ICH"



Clinical Trial Project Manager

Tags for this Online Resume: cGCP, ICH, FDA, Clinical trial, Core lab, Program manager, cGCP / ICH, ECG data

Clinical Research, Research Triangle Park

Savvy, analytical, highly organized and detail oriented individual in search of an interesting position within the realm of clinical trials research. Ideally, the position would allow me to take advantage of my understanding of biology, research methodology, experimental design and medical terminology. I am seeking a position that will lead to a clinical research associate position.

Tags for this Online Resume: Oncology, Clinical Trials, Analytical , Research, GCP/ ICH

Clinical Project Manager, Sacramento/San Francisco, CA

Tags for this Online Resume: Project Management, Monitor, GCP-ICH, FDA, Clinical Research, Patient Safety, 21 CFR 11, Data Management, Budget and Forecast Planning

Featured Profile

Senior Research Nurse Coordinator

I'm a competent, organized, detailed oriented and efficient Clinical Research Nurse Professional with 10 years experience and proven administrative skills. Experience includes OB/GYN, Vascular Surgery, Podiatric and Ophthalmology Reserach. Excellent communication skills and proficient in time management and problem solving abilities. Knowledge of GCP and ICH guidelines, regulatory requirements, and the clinical trial process.

Senior Clinical Research Associates

I want to ensure that sites that I monitor are completed accurately according to Code of Federal Regulations and GCP/ICH.

Clinical Research Associate - 10 plus years Dallas, Field Application Specialis/Fiels Service Engineer - 5 years plus, San Francisco & Dallas

I am a strong self-starter with over 10 years’ monitoring experience with monitoring phase I to phase IV for pharmaceutical companies, biotech companies and CROs. I also have over 5 years’ experience as a Field Application Specialist with a biotech company which is a similar position as a Pre-sales and Medical Device Expert at a biotechnology company. I work well independently or in a team environment. I am presently lookin...

Tags for this Online Resume: Dallas/Ft. Worth, TX, Clinical Research Associate, Regional Clinical Research Associate, GCP, ICH, FDA, Code of Federal Regulations, Clinical Research Studies, Therapeutic Areas

Senior Clinical Research Associatec

To be involved in clinical research

Tags for this Online Resume: clinical research associate, clinical team leader, senior clinical research associate, monitoring , FDA regulations, Phase 1- IV studies, site selection to site closeout, maintain GCP ICH compliance, GCP ICH compliance

Clinical Research Associate/Oncology-6 years experience- Philadelphia

Tags for this Online Resume: Oncology, clinical trials, EDC, medical teminology, CCRP, GCP/ICH

Featured Profile

Project Manager Delivering Quality and Timely Results

An ambitious, dedicated and accountable project manager who aims at delivering quality and timely projects. Claudia has high-standards and required experience to ensure projects are executed within projected budgets by maintaining cost management systems, through effective organization and management of resources and by conducting continuous analysis of project progress. She is a team leader on all of the department’s cli...

Ideal Companies: Johnson & Johnson, Merck, Pfizer, Quintiles, Amgen, Parexel, Hospital Corporation of America, Memorial Healthcare System, Therapeutics MD, Pharma

Tags for this Online Resume: Project Manager, EDC, CTMS, Financial Reports, Data Entry, Clinical Research

Senior Clinical Operations Supervisor - 11 years experience - GCP-ICH

Drug Safety Physician, Medical Monitor, 11 years experience

An accomplished individual offering long-term experience in the pharmaceutical industry. My areas of expertise include Medical Affairs, Drug Safety, Medical Monitoring, and Clinical Research Associate. Additionally, I possess 18-year medical practice including head and neck Oncology.

Tags for this Online Resume: Medical Monitor, PSUR, GCP/ICH, CRA, Remote, MedDRA coding, Adverse Events, Risk Management Plan, SMQ