About The Position

Seeking a highly organized and proactive Clinical Trials Director to help grow the clinical research program. This individual will be responsible for overseeing project timelines, managing milestones, and keeping the lead PI and other involved investigators on track across multiple studies/projects. Most important is keeping the projects on track, organized, and ensuring execution across all program components.

Requirements

  • Bachelor's degree in a related field.
  • Eight years of experience in clinical trials, including management and/or supervisory experience, or an equivalent combination of education, training and experience.

Responsibilities

  • Manages multiple clinical trials which may be at multiple locations.
  • Typically supervises a clinical trials staff of more than five.
  • Develops and implements strategies for business development.
  • Collaborates with administration to develop and implement strategic plans for clinical trials in specific clinical areas.
  • Tracks and manages finances for a large clinical research portfolio and manages expenses using Emory financial reporting tools.
  • Directly implements Standard Operating Procedures.
  • Facilitates contracts, budgeting, and routing of research studies that may include industry trials, NIH awards, and other funding mechanisms.
  • Has responsibility for quality assurance, record retention, and documentation flow.
  • Performs related responsibilities as required.
  • Coordinating research activities, managing communications across clinical sites.
  • Drafting protocols and supporting regulatory submissions.
  • Managing subcontracts, service agreements, and study budgets.
  • Leading meetings, tracking action items.
  • Hiring and supervising research staff.
  • Ensuring timely communication and task follow-through.

Benefits

  • Opportunity to work from home regularly.
  • Flexible weekly schedule based upon business needs.
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