Lensa
Clinical Trial Assistant
Summary
ICON plc is a healthcare intelligence and clinical research organization seeking a Clinical Trial Administrator (Clinical Trial Assistant) to join its team. The role supports the coordination and administration of clinical trials, helping ensure compliant and smooth trial execution while contributing to the advancement of treatments and therapies.
What you'll do
- Assist in coordinating and administering clinical trials in compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support preparation of study materials such as informed consent forms and case report forms.
- Collaborate with cross-functional teams to facilitate communication and smooth trial execution.
- Track and report clinical trial metrics and milestones.
Requirements
Bachelor's degree in a scientific or healthcare-related field.
Prior experience or strong interest in clinical research.
Knowledge of clinical trial processes, regulations, and guidelines.
Excellent organizational and communication skills.
Ability to work collaboratively in a fast-paced environment with attention to detail.
Conditions
Competitive salary (amount not specified).
Benefits may include annual leave, health insurance options, retirement planning, Employee Assistance Programme (LifeWorks), life assurance, and flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).
Inclusive and accessible workplace; reasonable accommodations available.