Site Services Specialist 1 (Icon)
5/26/20261 min read
Roles and Responsibilities
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%)
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