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Senior Clinical Trial Associate at ICON plc - ApplyBlast

Senior Clinical Trial Associate

ICON plc

4 months ago

Taipei, Taiwan

Hybrid

Full Time

Senior

0 applicants

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About this role

A Senior Clinical Trial Associate at ICON manages the administrative and operational execution of clinical trials, ensuring compliance with global regulations like GCP and ICH. Key duties involve preparing submission dossiers for ethics committees, coordinating responses to regulatory queries, and aligning study timelines with clinical research associates.

Responsibilities

Prepare and submit clinical trial application dossiers
Coordinate responses to ethics committee queries
Align study milestone dates with CRA teams
Maintain proper in-house TMF submission documents
Update and manage local study documentation

Skills

Qualifications

Bachelor's Degree in Life Sciences or related field

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.