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

Clinical Careers Page(1 month ago)

HybridFull TimeMedior$80,707 - $108,389 (estimated)Clinical Operations

About this role

The Study Start Up Associate II at ICON supports clinical trial site start-up for medical device studies, focusing on preparation and approval of regulatory documentation and ensuring compliance with applicable standards. The role collaborates with contract & budget and clinical teams and supports enrollment, follow-up and trial closure activities. The position is based in Arden Hills, MN with hybrid onsite expectations.

View Original Listing

Required Skills

IRB Submissions
ICF Negotiation
Regulatory Documents
eTMF
CTMS
Clinical Start-Up
Site Management
Regulatory Compliance
Document Tracking
Audit Support

+2 more

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.

View more jobs at Clinical Careers Page →