Clinical Study Manager

7 days ago


Canada ICON Plc Full time
Study Manager (SM) Role

As a Study Manager (SM) at ICON Plc, you will be a key member of the Global Study Team, contributing to delivering clinical studies to time, cost, and quality. Your role will involve overseeing study eTMF completeness, ensuring inspection readiness, and driving continuous improvement initiatives.

Key Responsibilities
  • Work closely with the Study Delivery Lead on end-to-end operational study delivery activities, from study setup to study archival.
  • Monitor study conduct and progress, identifying and resolving risks/issues that may impact delivery.
  • Facilitate and maintain interactions with internal and external partners to ensure successful study delivery.
  • Manage vendor relationships and oversee study-specific deliverables.
  • Coordinate study-related activities and manage study team communication.
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/scientific environment.
  • Excellent knowledge of ICH-GCP, clinical study delivery process, and industry standards.
  • Strong project management skills and good leadership skills.
  • Excellent communication and relationship-building skills.
What We Offer
  • Competitive compensation and benefits package.
  • Opportunities for professional growth and development.
  • Diverse and inclusive work environment.
  • Recognition and rewards for outstanding performance.


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