Senior Project Manager for clinical trials at ICON plc, interpreting complex medical data and managing project responsibilities. Leading sponsor communications and project coordination in a dynamic environment.
Responsibilities
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.
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