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Online Resumes with "study protocols"
Clinical Research - 7 Years of Experience - Near 94134
I am a Senior Drug Safety professional, board-certified in Ob-Gyne with 20 plus years career in the pharmaceutical/biotech industry. Experience with phase I - III clinical trials and post-market drug safety in US and international setting. Created full-service, compliant Drug Safety department beginning from phase III through approval and post-market surveillance (various therapeutic area targeted therapy). Experience with ...
Tags for this Online Resume: Pharmacovigilance, Drug Safety, Clinical Research, Clinical Project Management, Medical Affairs, Clinical Development
Laboratory Technician - 20 Years of Experience - Near 27705
Senior pharmaceutical research scientist with extensive experience working across a broad range of therapeutic areas and proven strengths in the development, validation, and standardization of animal models / in vivo paradigms. Demonstrated success in the development and execution of study protocols to monitor a broad range of physiological indices for the evaluation of drug effects
Clinical Research
Experienced Clinical Research Associate seeking a challenging and rewarding Clinical Research Associate (CRA) position that will utilize my clinical site monitoring and general management skills and experience to coordinate, monitor and manage all aspects of clinical trials in accordance with the ICH-GCP guidelines, FDA regulations, standard operating procedures and study protocol.
QA - 20 Years of Experience - Near 39426
Pharmacopeia upgrade monograph tests for Dimethyl Sulfoxide. * Monitor and update USOSHA and foreign country SDS sheets and product label / placard required for a wide array of products. * Played an integral role in securing the EU Certificate of Suitability (CEP) for Procipient Dimethyl Sulfoxide in 2014. and Health Canada Drug Master Files (DMF) for Dimethyl Sulfoxide to ensure compliance and enhance clarity. Maintained r...
Ideal Companies: 1 month -
Tags for this Online Resume: Audit, Pharmaceutical, Quality Assurance, Test, DMS, Dms (Data Mgmt Tool), QA/QC, ISO, Management, Instrumentation
Medical Scientist - 13 Years of Experience - Near 21136
HIGHLIGHTS OF QUALIFICATIONS: * 2+ years of clinical research monitoring experience and 25+ years pre-clinical experience * Knowledge of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines * Knowledge of FDA regulations * Knowledge of clinical trials for investigative biomedical and pharmaceutical studies. * Good working knowledge of Pharmacology, Epidemiology, Biology, Chemistry, Ph...
Tags for this Online Resume: Cancer, Leadership, Medical, Patient Care, Quality, Quality Assurance, Quality Control, Trauma, Troubleshooting, Phlebotomy
Team Leader - 9 Years of Experience - Near 08854
Experience Summary * A seasoned analytics and consulting professional with ~9 years of industry experience as a SAS Consultant and Business Data Analyst with a strong understanding of Data Handling and Management, SAS, Project management, and Business Analysis. Project Summary This program supports the in-out of the company's innovative value-based programs. This includes the analyses of business KPIs and financial metrics ...
Tags for this Online Resume: Programming, Support, ETL, QA, Management, Data Extraction, Project Management, Requirements Analysis, SAS, Data Analyst
Clinical Research - 18 Years of Experience - Near L4C 4J9
SUMMARY OF SKILL SETS * Clinical Research experience as an MD in Gastroenterology & Hepatology Department * Clinical experience as physician assistant in Pediatrics and Allergy & Asthma * Qualified in Medical Research, competence in assessing study-related literature and liaising with sponsors, writing medical proposals and publishing international medical articles in Medicine. * Detail oriented, analytical and timeline dri...
Tags for this Online Resume: Allergy, Immunization, PEDIATRIC, Pediatric Patients, Pediatrics, Medical, Protocol, Gastroenterology, Clinical Research, Homeopathy, Medical Researcher
Clinical Project Manager-6 years-France
I supervised the development of several clinical projects in different therapeutics areas and in different countries (France, England, Italy, USA and Canada). I coordinated the clinical activities in respect with the budget, timeframe and regulations (SOPs, FDA-GCP and ICH guidelines). I trained CRAs, site investigators and CROs to ensure study protocol comprehension and compliance (initiation visits, co-monitoring). I plan...
Tags for this Online Resume: clinical project, oncology, dermatology, cardiology
Clinical Research - 3 Years of Experience
Summary * Highly qualified clinical research professional with over 17 years' experience, including Phase I-IV domestic and international studies (including EU, Eastern EU, South America, Asia, and Canada) in a wide range of therapeutic areas. * Experienced in all stages of study development from start up to close out with ability to view study progress by each data point or from a more global prospective. * Skilled at effe...
Tags for this Online Resume: Clinical Research, Oncology, PEDIATRIC
Clinical Research - 7 Years of Experience - Near 10803
Qualification Highly motivated and accomplished Clinical Research Coordinator with extensive skills and experience. Nine years of experience as an Oncology research coordinator. Proven ability to manage multiple studies simultaneously. Managed phase 1b - IV protocols according to GCP and FDA guidelines. Experience as a supervisor and mentor to study coordinators across various oncology disease sites. Trained staff on study ...
Tags for this Online Resume: Appraisals, Audit, Clinical Research, Data Quality, Documentation, Management, Protocol, Quality, Quality Assurance, Recruiting
Clinical Research - 2 Years of Experience - With 15 years research experience Near 34609
SUMMARY OF EXPERIENCE Dedicated Clinical Research Associate with more than 10 years of experience in Clinical research. Broad background in clinical trials management of phase I/II/III/IV trials in Ophthalmology, Rheumatology/Immunology, and Endocrine including the implementation of study protocols, monitoring of sites and on-site data management and collection. Significant expertise in Ophthalmology Terminology, Treatments...
Tags for this Online Resume: CATARACT, Trauma, Triage, Clinical Research, Collection, Health Insurance Portability And Accountability Act, Research, Injections, Documentation, Monitoring
Clinical Research - 5 Years of Experience
Medical Doctor with Post Graduate training and Diploma in Clinical Research from AAPS Toronto * Over 14 years experience working in clinical environment. * Strong understanding of Clinical Research processes according to Study Protocols ICH/GCP
Tags for this Online Resume: Clinical Research, Management, Protocol, Research, Data Management, Good Clinical Practices, Medical, Clinical Trials, Informed Consent Forms, Study Reports, SOP, Regulatory approval
