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Study Start Up Associate I at ICON plc - ApplyBlast

Study Start Up Associate I

ICON plc

3 days ago

Warsaw, Mazowieckie, Poland

Onsite

Full Time

Junior

0 applicants

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About this role

The Study Start Up Associate I supports the operational aspects of clinical trial submissions under the Global/Local Clinical Trial Regulation per EU CTR in the Clinical Trial Information System (CTIS). This role involves assisting with document management, quality checks, and submission archiving while ensuring accurate tracking of submission statuses. The position requires collaboration with cross-functional teams to maintain compliance with regulatory requirements and support trial delivery timelines.

Responsibilities

Support operational aspects of clinical trial submissions in CTIS
Manage document collation, quality checks, and submission archiving
Track submission progress and maintain accurate data in clinical trial management systems

Skills

Qualifications

Bachelor's degree in life sciences or a related field

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

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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.