Clinical Trial Manager

Belcan

  • Mason, OH
  • 30+ days ago
  • $10.45 Per Hour
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Skills

  • Biologyunmatched
  • Budget Managementunmatched
  • Chemistryunmatched
  • Clinical Practices/Protocolsunmatched
  • Clinical Trialunmatched
  • Clinical Trial Managementunmatched
  • Drug Developmentunmatched
  • Expense Trackingunmatched
  • GCP (Good Clinical Practices)unmatched
  • ICH Regulationsunmatched
  • Logistics Managementunmatched
  • Network Integrationunmatched
  • Problem Solving Skillsunmatched
  • Quality Managementunmatched
  • Scientific Principlesunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Standards Developmentunmatched
  • Technical Deliveryunmatched

Description

Job Title: Clinical Trial ManagerLocation: Mason, OHZip Code: 45040Duration: 12 monthsPay Rate: $10.45 - $73.22/hr.Keyword's: #Masonjobs; #ClinicalTrialManagerjobs;Start Date: ImmediateJOB DESCRIPTION:Procedural work and expertise in Application work by combining hands-on experimentation with scientific principles and knowledge from science/engineering education to drive foundational technical understanding and solve technical problems. Delivers technical outputs which address critical innovation challenges and completion of key milestones. The Clinical Trial Manager (CTM) is a key member of the clinical team with responsibility for defining and managing the quality execution of clinical studies. Partner closely with product and technology development to design and execute clinical studies for claims support, credentialing, decision making, and fundamental understanding. The CTM role is pivotal for driving robust human testing and clinical trials that are compliant with established governance principles, including ICH-GCP Guidelines. Responsibilities: Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key components of a successful clinical trial. Management of study logistics, timelines, and budget/expense tracking. Prepare documentation for study placement and clearances, clinical trial protocols, and IRB submissions, as needed. Conduct study close out and tasks, including documentation and archiving of study materials. Contribute to the development of Standard Operating Procedures and adhere to all aspects of Governance and Quality systems. Represent clinical operations are regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed. Skills: Experience in human testing and the management of Clinical Trials, including a fundamental knowledge of Good Clinical Practices. The candidate will have a strong background in a fundamental knowledge of Biology, Chemistry and/or measurement science.Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

Numbers & Facts

LocationMason, OH

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