ICON plc
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
- Support Local Trial Managers (LTMs) and Site Managers with trial documentation and logistics
- Ensure regulatory documents are accurate, complete, and submitted on time
- Assist in site and country feasibility activities
- Maintain Trial Management Systems and eTMF documentation
- Collect and track Financial Disclosure Forms and training documents
- Support informed consent form (ICF) reviews and regulatory submissions
- Provide administrative support: meeting coordination, correspondence, filing, etc.
- Collaborate cross-functionally with legal, regulatory, and contracts teams
You are:
- Bachelor’s degree preferred (Life Sciences or related field)
- 0–2 years of relevant clinical trial experience
- Strong skills in MS Office (Word, Excel, Outlook, etc.)
- Excellent organization, multitasking, and communication skills
- Proficient in English
Why Join ICON?
At ICON, you’re not just starting a job — you’re building a career. You’ll join a culture of excellence and innovation, supported by a team that values integrity, respect, and accountability. From contributing to clinical breakthroughs to shaping the future of medicine, your work will matter.
Apply Today
Be a part of something bigger. If you’re passionate about clinical research and ready to grow in a globally respected organization, this opportunity is for you.
To apply for this job please visit careers.iconplc.com.
