Study Start Up Associate II - Medical Device - Arden Hills, MN

Clinical Careers Page(1 month ago)

HybridFull TimeMedior$73,331 - $98,836 (estimated)Clinical Operations

About this role

Study Start Up Associate II (Medical Device) at ICON supports clinical research by coordinating regulatory and administrative processes for site start-up of medical device trials. The role works with clinical teams, contract & budget functions, and external sites to ensure regulatory compliance and investigator readiness for studies based in Arden Hills, MN.

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Required Skills

Regulatory Submissions
IRB Submissions
ICF Negotiation
Document Control
eTMF
CTMS
Communication
Stakeholder Engagement
Compliance
Multi-Tasking

Qualifications

Bachelor's Degree

About Clinical Careers Page

iconplc.com

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.

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