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Study Start Up Clinical Research Associate at ICON plc - ApplyBlast

Study Start Up Clinical Research Associate

ICON plc

3 days ago

Nairobi, Kenya

Onsite

Full Time

Medior

0 applicants

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About this role

The Study Start Up Clinical Research Associate at ICON Strategic Solutions manages end-to-end site-level study start-up activities, from site selection through to activation, ensuring compliance with ICH-GCP and local regulatory requirements. This role serves as a key point of contact for investigational sites and internal teams to achieve start-up milestones efficiently. The position requires independent management of regulatory submissions, essential documentation, and stakeholder coordination to minimize activation delays.

Responsibilities

Manage end-to-end study start-up activities for assigned clinical trial sites
Coordinate regulatory authority and Ethics Committee submissions and resolve queries
Maintain study start-up systems and ensure inspection-ready TMF documentation

Skills

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

View Profile

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.