Site Engagement Liason

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 Clinical Trial Liaison at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key Responsibilities Include

- Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies.
- Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards.
- Foster strong relationships with study sites and investigators to enhance patient recruitment and retention.
- Act as a liaison between sponsors, investigators,



and study participants, providing support and guidance throughout the enrollment process.
- Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes.

Your Profile

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required Qualifications And Experience

- Bachelor's degree in a relevant field, such as life sciences or healthcare.
- Proven experience in clinical trial enrollment or related roles.
- Strong analytical and problem‑solving skills with the ability to interpret complex medical data.
- Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders.
- Detail‑oriented with a commitment to ensuring accuracy and compliance in all aspects of clinica

📌 Site Engagement Manager (España)
🏢 ICON Strategic Solutions
📍 España