Clinical Research Associate
4 days ago
At ICON, we are dedicated to making a positive impact on people's lives. We do this by working alongside our clients to deliver innovative solutions that help them develop life-changing medicines.
This role is an exciting opportunity for you to be part of a global team that plays a key role in the success of clinical trials at a local level.
- Provide administrative support to other members of the clinical study team, ensuring the smooth tracking of study progress.
- Collaborate with site staff to ensure clinical trials are conducted according to protocol.
- Manage documentation, track, and review electronic files.
- Be responsible for IRB/EC and RA submissions from initial submission to amendment.
- Support the study start-up process locally.
You will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients' lives.
Key Requirements:- Detail-oriented, passionate, and reliable.
- A relevant educational background in life sciences or as a licensed healthcare professional.
- Strong interpersonal skills.
- Proficiency in MS Office.
- The ability to manage multiple priorities simultaneously.
- A quality-focused mindset.
- Oncology trial experience is a plus.
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