Manage 10–15 clinical lab studies, act as sponsor contact and represent ICON at meetings. Ensure GCP compliance, reporting, and ICOLAB support to sponsor personnel.
Responsibilities
Ensure client satisfaction by acting as the Sponsor’s main contact person in all matters regarding ICON services including the day-to-day management of studies
Attend and represent ICON at Sponsor meetings
Manage 10-15 studies in accordance with Good Clinical Practice
Communicate with Sponsor’s study progress in a responsible and professional manner and provide Sponsors with regular management reports
Provide ICOLAB support to sponsor personnel
Design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies
Requirements
Bachelor's degree in a relevant field such as life sciences or healthcare
Previous experience in project management within a laboratory or clinical research setting
Strong communication and interpersonal skills, with the ability to represent the company at sponsor meetings
Ability to manage multiple studies concurrently while ensuring adherence to regulatory standards and guidelines
Detail-oriented with strong organizational skills to effectively manage study documentation and timelines
Knowledge of Good Clinical Practice (GCP) and study management
Benefits
Competitive salary
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
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments
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