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Clinical Research Associate - 5 years - Pennsylvania
I am a Documentation Specialist who has over five (5) years Clinical Research experience working for Contract Research Organizations (CROs) and Pharmaceutical companies performing the following clinical related activities; Registration & Results Disclosure, Data Integrity, Document Management, Project Management, Site Management, and Quality & Compliance.
Clinical Research
Clinical Research - 15 Years of Experience - Near 02906
QUALIFICATIONS SUMMARY Multi-faceted professional with solid background in various aspects of clinical research working on different perspectives in clinical research: on site, CRO and sponsor. Organized multi-tasker with excellent aptitude in the biosciences and analytic ability for problem solving. Strong communication and organizational skills. High attention to detail and accuracy. Team player who works effectively with...
Tags for this Online Resume: Query, Research, Management, Hematology, Oncology, Data Management, Email, Medical, Medical Records, Clinical Research
Clinical Research
Clinical Research
Tags for this Online Resume: clinical research, Public Health, epidemiology, biostatistics, medicine, management
Oncology Clinical Research and Informatics - 8 Years of Experience - Near 08852
Clinical Research
Clinical Research - 1 Years of Experience - Near 00977
Theory classes for MBBS I MBBS II BDS I BDS II and B.Sc Nursing Practical classes for MBBS I MBBS II BDS I BDS II and B.Sc Nursing Experience Summary: 5. * Worked as a Dental surgeon in Buddhasubba Dental Hospital, Itahari - 10 months * * * Major Strengths * Learning ability * Commitment * Adaptability * Counseling * Punctuality * Team building * Teaching ability * Flexibility * Dedication * Devotion Language and Degree of ...
Tags for this Online Resume: Hindi Language, Nursing
Clinical Research - 10 Years of Experience - Near 92115
Clinical Research - 12 Years of Experience - Near 07042
Professional Summary Over 11 years' experience in the Pharmaceutical Industry, focusing on Drug Safety, Regulatory Compliance, Clinical Trials, Protocol Initiation and Management, Data Standards and Maintenance, Study Management, Pharmaceutical Operations, and Basic Molecular Biology Techniques Core Qualifications * Knowledge of GCP's, ICH and FDA Guidelines * Project Development * Knowledge RECIST & CHESON criteria * Safet...
Tags for this Online Resume: Surgery, Clinical Science, Protocol Developement, Sarety Documentation, Study Management, Oncology, Toxicology, Regulatory Compliance
