Job Description: Clinical Operations Management is responsible for strategic oversight and leadership direction within the Clinical Operations function. Job Responsibilities: Coordinates the ordering, packaging, shipping and tracking of site supplies and materials Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines Support Project Managers in charge of medical device clinical trials Participates in file audits Performs remote and onsite monitoring visits as needed and according to Clinical Monitoring Plan. Creates and assists with maintenance of project files, handles project correspondence Manages shared mailbox, processes site requests and routes correspondence appropriately Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions Maintains, updates, and inputs clinical tracking information into databases Prepares and maintains site manuals, reference tools and other documents Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client Job Requirements: Bachelor's degree preferred or equivalent experience Experience in clinical research/pharma/biotech or related field Good knowledge of medical terminology, clinical data, and ICH/GCP/EU MDR preferred Ability to successfully prioritize and work on multiple tasks Strong attention to detail, accuracy and organizational skills Excellent communication, presentation, and interpersonal skills Ability to embrace new technologies Minimal travel up to 10% may be required Job Details: Company: Cardinal Health Vacancy Type: Full Time Job Location: Los Angeles, CA, US Application Deadline: N/A Apply Here careers-trivia.net
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