Organization Overview
inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing.Title
Senior Clinical Research AssociateResponsibilities
Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performanceMonitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet-i3 SOPs and/or client guidelines
Recruit investigators
Negotiate study budgets with investigators
Obtain, review, and process regulatory and administrative documents from investigator sites
Review and develop protocols
Review and develop CRFs
Coordinate and present at Investigators’ Meetings
Participate in proposal meetings with potential clients
Prepare and review Serious Adverse Event (SAE) reports
Prepare project management reports for clients, project personnel, and PharmaNet-i3 management
Resolve issues, questions, and requests for additional study supplies
Review and approve monitoring trip reports
Review and verify completed CRFs
Review clinical data in-house
Resolve queries of CRF data with study site personnel
Review Tables and Listings generated from study data
Author Clinical Study Reports
Train and mentor CRAs on monitoring, internal procedures, and query resolution
When allocated by study management, submit essential/required documents to a central IRB or a country’s central Ethics Committee, and, if necessary based on local requirements, the Competent Authority.
Requirements
Bachelor’s Degree or nursing credentialover three and a half years experience in clinical research and direct monitoring experience required.
Fluent in English
Ability and willingness to travel 50% of the time
Excellent organizational skills
Ability to manage time and work independently
Excellent written and oral communication skills
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