Clinical Regional Project Lead

Posted 1hrs ago

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Job Description

Regional Clinical Project Lead managing oncology clinical trials for PSI, a contract research organization. Supervising country-level teams, sites, monitoring, regulatory submissions, and study delivery.

Responsibilities:

  • Oversee, manage, and coordinate project team activities in designated countries and ensure consistency of Clinical Operations processes across regions
  • Plan, implement, and manage projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents
  • Act as primary or secondary project management contact for project teams and PSI support services in designated countries
  • Review study status and provide progress reporting when delegated by the Project Manager
  • Collect and report project status updates for designated regions internally and externally
  • Develop and update project planning documents, essential study documents, and project manuals/instructions
  • Manage and report KPIs for designated countries and clinical project team members
  • Ensure project timelines and subject enrollment targets are met
  • Coordinate study-specific and corporate tracking systems
  • Coordinate site contractual startup and budget negotiations
  • Establish project-team communication lines and supervise clinical project team members’ performance
  • Identify, escalate, and resolve resourcing and performance issues
  • Conduct or supervise therapeutic-area training and prepare Investigator presentations
  • Ensure compliance with project-specific training matrices
  • Perform field training of Monitors tailored to project needs
  • Supervise site selection, site initiation, routine monitoring, and closeout visits
  • Oversee investigator and site payments, CRF data retrieval/upload, monitoring, and query resolution
  • Supervise preparation for study audits/inspections and resolution of findings
  • Coordinate supervised monitoring visits and review site visit reports
  • Coordinate initial and follow-up Regulatory and Ethics Committee submissions and notifications
  • Oversee safety information flow and participate in feasibility research
  • Review and approve project-related expenses and timesheets when delegated by the Project Manager

Requirements:

  • College/University degree in Life Sciences or equivalent combination of education, training, and experience
  • Prior experience in Clinical Research and on-site monitoring
  • Prior experience monitoring within the US
  • Experience as a Study Manager/Clinical Trial Manager, with ability to supervise project activities as a Regional Lead or equivalent
  • Experience in Oncology
  • Full working proficiency in English
  • Proficiency in MS Office applications, including MS Project
  • Communication, presentation, and customer-service skills
  • Ability to negotiate and build relationships at all levels
  • Team-building, leadership, and organizational skills

Benefits:

  • Remote work
  • Career advancement opportunities
  • Hands-on involvement in every aspect of clinical studies
  • Opportunity to lead challenging full-service projects
  • Work with a company that puts its people first