Site Services Specialist I

As a Site Services Specialist I at ICON, you will support clinical trial sites by managing logistics, resolving site-related issues, and ensure that sites are equipped with the necessary resources to conduct trials effectively.

What You Will Do:

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

• Providing logistical and operational support to clinical trial sites, ensuring timely and efficient delivery of materials and supplies.

• Assisting in resolving site-related issues, troubleshooting operational challenges, and ensuring adherence to study protocols.

• Collaborating with cross-functional teams to ensure seamless communication between trial sites and ICON teams.

• Tracking site performance metrics and providing reports to support study timelines and goals.

• Ensuring compliance with Good Clinical Practice (GCP) and applicable regulatory requirements across all site activities.

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, healthcare administration, or clinical research.

• Experience in site management, clinical operations, or a related field is preferred.

• Strong problem-solving and organizational skills, with the ability to manage multiple tasks and deadlines.

• Knowledge of clinical trial processes, GCP, and regulatory requirements is a plus.

• Excellent communication and interpersonal skills, with the ability to work effectively within a cross-functional team.

• Willingness to travel as required (approximately 1%)