Live opening · Posted 9 hours ago

Site Specialist

ICON plc · 2 Locations
Workday
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At a glance

The key details from the original listing.

Posted 9 hours ago
CompanyICON plc
Location2 Locations
SourceWorkday
ListedPosted 9 hours ago

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About the role

Description supplied by the original job listing.

Site Specialist II - India, Chennai - Office with Flex
ICON is a global 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.
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 multiple priorities with attention to detail.
Excellent communication skills—both written and verbal—with the ability to liaise effectively across global teams.
Familiarity with ICF customization, translation workflows, IRB/EC submission processes, and contract negotiations is highly desirable.
Willingness to work flexible shifts to align with global team needs.
#LI-KT1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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