Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified
IQVIA Biotech is growing! Our team in Brazil has openings for Clinical Project Coordinators. This role can be home-based anywhere in Brazil. Job Overview Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Summarized Purpose : Manages, coordinates and evaluates medical projects for one or more programs in collaboration with management and other stakeholders to ensure consistency, alignment, and compliance of internal processes
Education and Experience : - Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or - Direct experience in safety/Pharmacovigilance (comparable to
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Medical Director – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Summarized Purpose: Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings,
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