Clinical Study Manager

7 days ago

Canada ICON Plc Full time
Study Manager (SM) Job Description

At ICON Plc, we are seeking a highly skilled and experienced Study Manager (SM) to join our Global Study Team. As a key member of the team, you will play a critical role in delivering clinical studies to time, cost, and quality.

Key Responsibilities:

  • Oversee study conduct and progress, identifying and resolving risks and issues that may impact delivery.
  • Develop and maintain study plans, including monitoring plans, vendor management plans, and risk management plans.
  • Collaborate with internal and external partners to ensure successful study delivery, including regulatory, quality assurance, and CROs.
  • Manage vendor relationships and oversee study-specific deliverables.
  • Coordinate study-related activities, including meetings, communication, and data management.
  • Ensure study inspection readiness, including eTMF completeness and quality.
  • Manage study budgets and expenses, including task orders and change orders.

Requirements:

  • University degree or equivalent in a medical or biological science or related field.
  • At least 3+ years of relevant work experience in a pharmaceutical or scientific environment.
  • Excellent knowledge of ICH-GCP, clinical study delivery process, and industry standards.
  • Strong project management skills, including analytical and financial skills.
  • Excellent communication and relationship-building skills.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunities for career growth and professional development.
  • Diverse and inclusive work environment.
  • Recognition and rewards for high performance.

How to Apply:

If you are a motivated and experienced Study Manager looking for a new challenge, please submit your application, including your resume and cover letter, to [insert contact information].

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