Site Engagement Liason
ICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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 clinical trial enrollment.
Employment with ICON is contingent upon having the
📌 Site Engagement Manager (Madrid)
🏢 IRE
📍 Madrid