Clinical Study Manager

6 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 be responsible for delivering clinical studies to time, cost, and quality, ensuring inspection readiness, and driving continuous improvement initiatives.

Key Responsibilities:

  • Oversee study eTMF completeness, including setup, periodic reviews, and following up on missing documents.
  • Work closely with the Study Delivery Lead to ensure end-to-end operational study delivery activities, from study setup to study archival.
  • Collaborate with internal and external partners to manage clinical study management activities, including vendor management and CRO oversight.
  • 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.

Requirements:

  • University degree or equivalent in medical or biological science or a 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, including analytical and financial skills.
  • Excellent communication and relationship-building skills.

What We Offer:

  • Competitive compensation and benefits package.
  • Opportunities for professional growth and development.
  • A diverse and inclusive work environment.
  • Recognition and rewards for outstanding performance.

How to Apply:

Please submit your application, including your resume and a cover letter, to [insert contact information]. We thank all applicants for their interest; however, only those selected for an interview will be contacted.

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