Laboratory Project Lead – Clinical Trials

KCR Placement

Center Square (PA)

Remote

USD 110.000 - 140.000

Vollzeit

14 Tage+

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Benefits dieser Stelle

Health insurance
Life insurance
Retirement plan
Global Employee Assistance Program

Zusammenfassung

ICON is a global healthcare intelligence and clinical research organisation committed to bringing new medicines to patients faster. As a Senior Project Manager, Laboratory at ICON, you will oversee laboratory operations workstreams, ensure quality and on-time delivery, and lead cross-functional teams across studies.

You'll represent the client in meetings, manage budgets and study documentation, and ensure adherence to Good Clinical Practice standards throughout the project lifecycle.

Qualifikationen

  • Bachelor's degree in life sciences or healthcare required.
  • Minimum 5 years in clinical laboratory, clinical trials, or related roles.
  • 3+ years in project management for clinical trials or service areas like IVRS, distribution, or data management.

Aufgaben

  • Oversee laboratory operations workstreams ensuring quality and timely deliverables.
  • Act as client’s main contact for ICON Central Laboratories services.
  • Represent PM leadership in internal and client meetings; manage study updates.
  • Ensure studies adhere to Good Clinical Practice and regulatory requirements.
  • Coordinate protocol amendments, CLW completion, and data systems entries.
  • Monitor study progress and budgets; escalate issues as needed.

Kenntnisse

Leadership
Communication
Organizational skills
Travel readiness

Ausbildung

Bachelor's degree in life sciences or healthcare

Jobbeschreibung

ICON is a global healthcare intelligence and clinical research organisation committed to bringing new medicines to patients faster. As a Senior Project Manager, Laboratory at ICON, you will oversee laboratory operations workstreams, ensure quality and on-time delivery, and lead cross-functional teams across studies.

You'll represent the client in meetings, manage budgets and study documentation, and ensure adherence to Good Clinical Practice standards throughout the project lifecycle.

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