Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites for GCP compliance according to inVentiv Health SOPs and/or client guidelines
Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence and expense reports
Recruit investigators for participation in clinical trials
Conduct project feasibility assessments
Negotiate study budgets with investigators
Obtain, review for ...
My client is leading Japanese pharmaceutical company that has been providing innovative medicines essential to human health for 130 years. They are a unique and entrepreneurial mid-sized pharmaceutical company that develops and commercializes pharmaceutical products that address unmet medical needs, specifically in:
My client has a distinguished history in developing innovative therapies that address unmet medical needs. With its core business of ...
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects throughout the western region in accordance with applicable SOPs. Responsibilities include:
Performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational ...
Well-established Biologics company seeks 5+ years experience, providing program and project management support for clinical development of Oncology therapeutics.
** Clinical operations leadership, including Bio-banking methodologies, bio-marker, and companion diagnostics co-development.
** Protocol development, approval and adherence
** Oversight of sample collection and management activities
** Development, maintenance, and regulatory compliance of SOP's
Minimum BS ...
Feb 7 -
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