Become familiar with ICON’s SOPs/WPs, ICH GCP guidelines, appropriate regulations and ICON systems
Maintain timelines and ensure accuracy and completeness of data entered into ICON systems
Serve as a contact for sites and investigators participating in Clinical studies
Conduct and completes remote general administrative support for ongoing clinical trials
Take responsibility for project tasks and sees these tasks through to successful completion, with support.
Maintain a professional interpersonal relationship with study team, sites, and Sponsors
Participate in QA Audits as needed.
Regularly attend project specific and departmental meetings
Maintain Sponsor and patient confidentiality
Strong organizational skills
Other duties as assigned
Requirements
Minimum Bachelor's degree in a life science or related field preferred
Prior experience working in a clinical or healthcare environment is an advantage (e.g., internships, student roles, research support)
Understanding of ICH GCP Compliance
Excellent communication in German and English
Excellent organizational skills
A phenomenal teammate
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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