Site Specialist II - India, Chennai - Office with Flex
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring recent 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.
We are currently seeking a Site Specialist II to join our high-performing and collaborative Site Activation team at ICON. As a Site Specialist II, you will play a critical role in the start-up, maintenance, and contract management activities for clinical trial sites. This is an exciting opportunity to work across essential site-level functions that support the timely and compliant activation and maintenance of clinical sites globally.
What You Will Be Doing:
- Supporting Study Start-Up activities, including review of essential documents, green light process management, and site activation readiness.
- Handling maintenance tasks such as customization of site-specific Informed Consent Forms (ICFs),
coordination of translations, EC/IRB submissions, and documentation in eTMF systems.
- Assisting in the contract process, including understanding site contract workflows, managing contract amendments, participating in negotiations, and ensuring finalization of executed agreements.
- Collaborating effectively with cross-functional teams and stakeholders to ensure timelines are met and compliance is maintained.
- Communicating clearly and confidently with both internal and external teams, demonstrating excellent written and verbal communication skills.
- Working flexible hours to support global operations.
Your Profile:
- Bachelor’s degree in life sciences, business, or a related field.
- 3+ years of experience and solid understanding of study start-up processes, maintenance activities, and contract management in clinical trials.
- Strong organizational skills and the ability to manage multi
📌 Site Specialist (Bengaluru)
🏢 IRE
📍 Bengaluru