Strategic Clinical Project Director

Lotus Clinical Research, LLC

Northern (KY)

Hybrid

USD 120,000 - 180,000

Full time

9 days ago
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Job summary

Lotus Clinical Research, LLC is seeking a Project Director to provide leadership for assigned clinical programs. You will manage budgets, timelines, and deliverables while coordinating with sponsors, internal teams, and external partners.

The role may involve escalation support and governance for processes across projects. The position requires a Bachelor’s degree in life science/healthcare and extensive clinical research experience, including CRO exposure and FDA submission knowledge, with

Qualifications

  • Bachelor’s degree in life science or healthcare.
  • 4+ years of experience in clinical project management (investigational site, pharma, or CRO).
  • 8+ years of experience in clinical research.
  • Prior CRO experience and experience supervising projects is highly desirable.
  • Knowledge of FDA submission processes is required.

Responsibilities

  • Lead and support project teams; oversee budgeting, timelines, and deliverables.
  • Act as escalation point between sponsors, team members and cross-functional orgs.
  • Coordinate resources and governance for assigned programs and projects.
  • Facilitate development and implementation of project management processes and tools.
  • Participate in hiring and mentoring of project management staff as needed.

Skills

Team leadership
Project coordination
Multi-tasking
Communication
Can-do attitude
MS Office

Education

Bachelor’s degree in life science/healthcare

Tools

Microsoft Office

Job description

Lotus Clinical Research, LLC is seeking a Project Director to provide leadership for assigned clinical programs. You will manage budgets, timelines, and deliverables while coordinating with sponsors, internal teams, and external partners.

The role may involve escalation support and governance for processes across projects. The position requires a Bachelor’s degree in life science/healthcare and extensive clinical research experience, including CRO exposure and FDA submission knowledge, with

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