Clinical Trial Project Manager - Dallas, TX

Medpace, Inc.•Irving, TX
•Hybrid

About The Position

Medpace is seeking to hire established Clinical Trial Managers / Project Managers to join their Clinical Trial Management Group in Dallas, TX. The role focuses on managing day-to-day operations of clinical trials, serving as the primary contact for sponsors, and ensuring compliance with regulations. The company specializes in therapeutic areas such as Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, and Neuroscience. Medpace offers a competitive salary, bonus program, and equity grants.

Requirements

  • Bachelor’s degree in a health-related field
  • Experience in Phases 1-4
  • 3-5 years as a project/clinical trial manager within a CRO
  • Management of overall project timeline
  • Strong leadership skills

Nice To Haves

  • Advanced degree in a health-related field
  • Phases 2-3 preferred

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

Benefits

  • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Company-sponsored social events
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