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Senior Study Start Up Associate at ICON plc - ApplyBlast

Senior Study Start Up Associate

ICON plc

4 months ago

Paris, France

Hybrid

Full Time

Senior

0 applicants

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About this role

As a Senior Study Start Up Associate at ICON, you will work within a fast-paced clinical research environment to lead site start-up and activation tasks with a focus on quality and continuous improvement. You will support the Team Lead in executing country and site distribution plans while providing specialized expertise to drive project success. Key activities include conducting feasibility assessments, negotiating site contracts, ensuring regulatory compliance, and safeguarding patient welfare through informed consent documentation review.

Responsibilities

Lead site start-up and activation tasks requiring technical depth
Conduct feasibility assessments and site identification for trials
Negotiate site contracts and ensure regulatory guideline compliance
Review and finalize patient informed consent documentation
Provide specialized expertise to team leads and project managers

Skills

Qualifications

Bachelor's degree in Medical or Science field3 years of experience in clinical study start-up requirements

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.