Lorven Technologies Inc.

Clinical Trials Manager -- Fulltime -- Cincinnati, OH (Onsite)

Job Title: Clinical Trials Manager

Location: Cincinnati, OH (Onsite)

Duration: Fulltime

Job Summary

  • The Client is the leading CRO for Biotech companies and is continuing to add established Project Managers to join our Clinical Trial Management Group.
  • Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more.

Responsibilities

  • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables
  • Maintain in depth knowledge of protocol, therapeutic area, and indication
  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
  • Develop operational project plans
  • Manage risk assessment and execution
  • Responsible for management of study vendor
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Qualifications

  • Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred
  • Experience in Phases 1-4; Phases 2-3 preferred
  • 5+ years as a project/clinical trial manager within a CRO; required for home-based
  • Management of overall project timeline
  • Strong leadership skills
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Research, Analyst, and Information Technology
  • Industries

    Wellness and Fitness Services and Hospitals and Health Care

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