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Online Resumes with "GCP "
•Exacting, highly organized researcher with more than 12 years of combined experience in the pharmaceutical industry and university-based clinical pharmacology settings. •Experienced in investigation of Mechanism of Action of novel immunobiologics in investigator-initiated and clinical studies using disease-related biomarker selection and analyses. •Strong background in designing and conducting studies pertaining to the ...
Ideal Companies: Biotech companies
I have completed a Masters program in Biotechnology. I have keen interest in Clinical Research and Regulatory Affairs. I am looking for an entry level Clinical or Regulatory position. I have research site coordination experience in the areas of Rheumatology and Pain research. I am also ICH and GCP certified.
Tags for this Online Resume: CRF writing, patient follow up, administering informed consent form, administering psycometric scales, source documents review, Reporting SAEâ€™s, Pre-screening and recruiting patients, -Submitted documents to the Ethics Committee, Rheumatology, Pain
I thrive on learning new things and constant changes. Leading edge does not turn me away. Currently working in Switzerland and seriously looking to relocate to Asia for good opportunity.
OBJECTIVE: To obtain a challenging position utilizing my medical education and research background. Continue development of experience in pharmaceutical industry that includes data coordination, statistical analyses, GCP/ICH certification, and excellent verbal and written communication skills. Application of knowledge of clinical trial designs to trial execution in a CRA or project management role
Tags for this Online Resume: oralce, oncology, neuropharmacology biotech pharmaceutical, OBJECTIVE: To obtain a challenging position utilizing my medical education and research background. Continue development of experience in pharmaceutical industry that includes data coordination, statistical analyses, GCP/ICH certification, and excellent verbal and written communication skills. Application of knowledge of clinical trial designs to trial execution in a CRA or project management role
Management of Clinical trials quality
Obtain a position that will allow me to utilize my quality organizational skills, communication skills, educational background, and ability to work well with people in a team enviroment.
To utilize my vast knowledge and theraputic background in an exciting and challenging enviornment.
Tags for this Online Resume: MS Word, MS Excel, MS Outlook, MS Power Point, Adobe, FDA/ICH GCP, Siebel Clinical, Oracle Clinical, Lotus Notes, PHASE FORWARD, MediData Rave, ClinPhone, Master Scope CT, Livelink
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.
Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS â€¢ Knowledgeable in all areas of research including...
I have strong clinical research industry qualifications. I am seeking a position that is either in Richmond VA or can be done from my home office. I have been part of many successful projects and look forward to future successes!
Result-driven executive (18+ years, 35 Clinical Trail Designs and recruiting more than 3000 patients) with expertise commissioning and leading technology-based, Multi-million dollars revenue and growth initiatives ground solidly on business and economic value. As a Team Builder with extensive Clinical biostatistics (PK/PD, Clin. Operation & Clin. Trials), compliance with GCP, cGMP, and regulatory guidelines, Drug Developmen...
Tags for this Online Resume: RESEARCH AND DEVELOPMENT, PRECLINICAL PHARMACOLOGY, CLINICAL PHARMACOLOGY RESEARCH, CLINICAL PHARMACOLOGY RESEARCH, CLINICAL PHARMACOLOGY RESEARCH, CLINICAL PHARMACOLOGY RESEARCH, REGULAR AFFAIRS, REGULAR AFFAIRS, REGULAR AFFAIRS, REGULAR AFFAIRS
Implemented knowledge of ICH GCP and CDISC Standards. Proven organizational skills with the ability to learn quickly; excellent time management, meet tight deadlines; manage multiple tasks and changing priorities while working in a high-pressured environment. Reputable for my attention to detail skills and strong ability to respond and solve problems in real time to fulfill customer expectations. Ability to work effectively...