Key skills
Project Management
About this role
Role Overview
- Design and analyze clinical trials
- Interpret complex medical data
- Act as the sponsor’s main contact person in all matters regarding central laboratory services
- Review newly assigned protocols and Amendments
- Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW)
- Monitor study progress throughout the study using ICON tools
- Provide Sponsors with study management reports
- Proactively monitor study budget
- Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting Bid Defenses, or Initiations.
Requirements
- Bachelor's degree or local equivalent in science, or related field.
- Minimum of 5 years of experience in a clinical laboratory, clinical trials, or customer management role in a life science related organization.
- Minimum of 3 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical supply packaging and distribution, medical imaging, data management.
Benefits
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.