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Online Resumes with "GCP"



Clinical Research Compliance Professional - BSN

Operating Room RN with more than 12 years’ in clinical research/regulatory and emphasis on safety monitoring, review and analysis.

Tags for this Online Resume: BSN, nurse, safety, adverse events, clinical trial, research, educator, ICH-GCP, FDA, IRB, regulatory affairs, medical record review

Clinical Research Professional- 20 years experience- Memphis

Clinical research professional with over 20 years of experience in both industry and academia. Responsible for all audit activities for multiple phase 1-3 clinical trials. Responsibilities include but are not limited to ICH/GCP compliance. Reviews key study documents such as protocols, informed consents, CRFs, monitor reports, and CSR. Presents protocol and GCP training at Investigator meetings. Mentors and trains junior qu...

Tags for this Online Resume: GCP, FDA submission documents, Drug safety, GLP, NDA, Auditor

Featured Profile

PhD Research Scientist With 12+years of Experience in Biomedical Sciences

I am seeking opportunities to contribute as a scientist within preclinical drug development or drug discovery research for the bio-pharmaceutical industry to support the primary or secondary screening and characterization of the molecular mechanism of action of lead drug candidates enabling target validation. I specialize in the development of cell-based assays using genomic, proteomic and biochemical approaches implementin...

Ideal Companies: Biogen Idec, Joule Scientific, Novartis NIBR, Aveo Oncology, Agios, Pfizer, Millipore, Merck, EMD serono, Third rock ventures, Cambridge Scientific, Alkermes, Enlight Biosciences

Tags for this Online Resume: Lentiviral Retroviral shRNA RNA knockdown screens, Flow Cytometry, RTPCR, Immunopreciptations, Reporter assays, Cell based Assays, ELISA, Migration, Stable and Transient Transfections, Genomic and Proteomic Studies, Cloning, Transient siRNA knockdowns, Phenotyping Mammalian cell lines, Gene Overexpression, Subcloning to expression Vectors, Construct Stable Inducible Cell lines, Protein Kinase Assay, Pulse Chase Experiments, Transfection, Transduction, Transformation, Polyoma virus DNA tumor virus replication, Research Scientist, Cell Biology Protein Biochemistry Genetics Molecular Bioliogy Oncology Virology, FACS

Clinical Research Coordinator - 3 years of experience - indianapolis

I am a foreign medical school graduate who has 3 years of experience in cardiovascular, pulmonology, endocrinology and metabolic disease areas. I am looking to expand my career in research in which I can apply my knowledge for the benefit of the project. I am trained in vascular technology, vascular interpretation, BLS, ACLS, GCP, ekg tech, med assisting, and phlebotomy.

Featured Profile

Clinical Research Associate

 John is detail oriented, highly dependable previous site monitor and study coordinator with 4 years and 6 months experience, including assistant project management in the pharmaceutical development industry  He has attained knowledge and experience in 4 years of hands on provision of care for elderly and disabled persons assisting them with activities of independent daily living as well as dealing with transitional aspec...

Ideal Companies: Alcon, Merck, Wythe, Pfizer, Bristol-Meyers Squibb, Covance

Tags for this Online Resume: in-house monitor, Clinical Research Associate

Clinical Trial Associate

Tags for this Online Resume: research, clinical, regulatory, IRB, investigator, GCP

Clinical Research Associate

Dedicated, outcome-focused, and skilled professional with broad-based perception and exceptional skills in clinical research, encompassing trial monitoring, site management, audits, and detailed record keeping. Interested in pursuing a challenging career as a Clinical Research Associate to utilize commendable multitasking proficiencies and technical documentation expertise. Commended for demonstrating a collaborative leader...

Tags for this Online Resume: ICH/GCP, Clinical Research Associate, CRA

Clinical Research Manager - 11 years experience - charleston

I am a trained Epidemiologist/Public Health Scientist with over 10 years of experience in grant writing, project management, conduct of clinical trials, quality control management, and training/education of clinical researchers. I serve as a consultant to other researchers in the study design, conduct, and analysis of clinical research.

Tags for this Online Resume: Epidemiologist, Clinical trials research, grant writing, project management, IRB/GCP, statistical analysis

An accompished quality assurance professional - 25 years experience in GMP & GCP

A quality assurance professional with over 25 years experience in the areas of auditing , Good Clinical Practices and Good Manufacuring Practices and project managment. As a quality professional strong knowledge of quality standards for controlled document managment, corrective action and process deviations, and internal and external auditing.

Clinical Research Associate, Chicago, IL

I have been working in the Biotechnology industry for the last 9 years in the Pharmacokinetics & Drug Metabolism group at Amgen. I worked to characterize the pharmacokinetics (PK), pharmacokinetics/pharmacodynamics (PK/PD), and metabolic fate of novel drug candidates using state-of-the-art procedures and technologies. I supported discovery from research into the clinical. I developed and validated analytical methods whic...

Agricultural Technician

I am Compliance Auditor, with over 8 years of GLP and GCP experience from Amgen.