Clinical Trial Administrator
hace 4 semanas
At ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a skilled Clinical Trial Administrator to join our diverse and dynamic team.
This role will play a pivotal part in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Key Responsibilities:
Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
Support the preparation of study-related materials, such as informed consent forms and case report forms.
Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
Contribute to the tracking and reporting of 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.
What ICON Offers:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of benefits, including various annual leave entitlements, health insurance, competitive retirement planning, and a global Employee Assistance Programme.
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