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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Study Support Assistant at ICON, you will provide administrative and operational support for clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do:
You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
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- Assisting with the preparation and distribution of study documents, including protocols, informed consent forms, and regulatory submissions.
- Coordinating study-related meetings and maintaining meeting minutes and action items
- Managing study-related correspondence,
including emails, phone calls, and faxes.
- Supporting study teams in the maintenance of study files and documentation, ensuring compliance with regulatory requirements and company procedures.
- Assisting with the tracking and management of study-related materials and supplies.
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
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- High school diploma or equivalent required; Bachelor's degree preferred.
- Previous administrative or clerical experience, preferably in a healthcare or clinical research setting.
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal skills, with the ability to work effectively in a team environment.
- Proficiency in Microsoft Office suite (Word, Excel, Outlook).
- Willingness to travel as required (approximately 5%
📌 Study Support Assistant (Barcelona)
🏢 Icon Clinical Research
📍 Barcelona
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