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Online Resumes with "ICH GCP "
Clinical Research - 1 Years of Experience - Near 56003
To be part of an organization that is thriving on the latest technology, which gives a challenging career, in terms of accomplishing the responsibilities, where I can optimize exposure, vertical and communication skills. Also, to improve myself by continuous learning in and outside the purview of my responsibilities such that I can contribute to the progress of the organization.
Tags for this Online Resume: ADR reporting , ICH GCP, P.V, English Language, Hindi Language, regulatory affairs, protocol writing, article, leaflet, literature writing
Clinical Research Associate - Entry level - Waterloo
Driven, dynamic, and detail oriented. Trained in ICH/GCP guidelines to monitor clinical trial processes. Actively seeking an entry level CRA position within clinical trial programs.
Tags for this Online Resume: ICH/GCP, Clinical Research, SOPs, Case Report Forms, Microsoft Office Suite, Phases I - IV trials, Recruitment
Clinical Research - 7 Years of Experience - Near 40009
Tags for this Online Resume: Source data verification, ICH GCP, Site monitoring, CRF review, Communication with site, Ethics committee and sponsor, compliance to protocol
Clinical Pharmacovigilance/Drug Safety - 2 Years of Experience - Near 27713
Tags for this Online Resume: FDAguidelines, Medical writer, ICH GCP, Essential documents, Regulatory guidelines, E3 guidelines, Investigator brochure, ICF
Documentation
Seek challenging opportunity. My work experience and qualifications are diverse and include 10 years contracting to the Pharmaceutical Industry. Recently, I’ve earned applicable Clinical Trial subject matter certificates e.g., Kriger Research Group International (KRGI): Clinical Research Professional ICH/GCP – Certificate 9/2009; KRGI: Medical Terminology Program – Diploma 1/2010; Allied Schools: Pharmacy Technician Progra...
Tags for this Online Resume: Documentation
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.
Clinical Research
SUMMARY: * POST-MARKETING REPORTING: Vast clinical experience in reporting post-marketing events in the pharmaceutical industry. * CDM: Acquaintance on clinical data management, pre-clinical and clinical trials (Phase I, II, III and IV) * CLINICAL WRITING & DOCUMENTATION: Create clinical project documents according to the protocol, including, but not limited to, source documentation forms and guidelines, monitoring Standard...
Tags for this Online Resume: Ipc, Planning, Protocol, Research, Reuters, Business Planning, Coding, Documentation, Immunology, Information Technology
Clinical Research - 15 Years of Experience
Focused on obtaining a position as a Clinical Research Associate. Detail oriented with the ability to plan organize coordinate and manage projects according to priorities. Ongoing and consistent promotion of team work efforts. Excellent Communication and Interpersonal skills. Excellent oral and written communication skills with the ability to communicate effectively with medical personnel. Quick learner with the ability to ...
Tags for this Online Resume: Documentation, Management, Cardiovascular, Cardiology, Clinical Research, Distribution, Good Clinical Practices, Research
Clinical In-house Monitoring - 4 Years of Experience
Seeking a position in a globally focused organization that will utilize my qualifications while offering several opportunities to integrate personal enrichment with professional goals.
Tags for this Online Resume: Clinical Research, ICH GCP Guidelines, Schedule Y, eCRF, EC Submission, Site coordination, Inspection, Project Coordination
Clinical Data Management - 9 Years of Experience - Near 01821
SUMMARY * I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have 12 years of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 10 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I am experienced with all aspects of data management including project management, edit check...
Tags for this Online Resume: Management, Data Management, Pharmaceutical Industry, Quality, Quality Control, Team Lead, Document Management, Audit, Training, Quality Assurance
Clinical Research with 7 years of experience in medical field for different positions - Near M1G 3S4
Actively looking for an opportunity to work as a Clinical Research Coordinator. Recently completed the Placement as a Clinical Research Trainee from Toronto Rehabilitation Institute (UHN), Toronto on Sep 30, 2016. Key-Skills: * Possesses Post graduate Diploma in Clinical Research with medical background and experience of working in health field for more than 7 years * Well-developed time management skills and excellent atte...
Tags for this Online Resume: Data Entry, Medical, Health Awareness, Training, Cardiopulmonary resuscitation (CPR), Clinical Research, Phlebotomy, ICH-GCP Guidelines, Pharmaceutical Industry, Patient Recruitement, Clinical Trial
Clinical Research - 2 Years of Experience - Near 77449
HIGHLIGHTS OF QUALIFICATIONS: * RN with close to 2-years experience in clinical trials monitoring * Knowledgeable of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines and FDA regulations * Conversant with Design and Review of case report forms (CRF) * Conversant with Site Monitoring visits (PSVs, SIVs, IMVs and COVs) to meet study expectations. * Clinical and post-marketing safety ...
Tags for this Online Resume: Direct Patient Care, DRESSING CHANGES, Medical, Patient Care, Suctioning, Surgical, Wound Care, Acquired Immune Deficiency Syndrome (AIDS), HIV, Monitoring
