Site Specialist II

Clinical Careers Page(1 month ago)

HybridFull TimeMedior$91,853 - $122,415 (estimated)Clinical Operations

About this role

A Study Start Up Associate II at ICON is a mid-level clinical research professional based in Mexico City supporting the study start-up function within a global CRO. The role operates on a hybrid schedule and works with internal study teams and external site partners to enable clinical study initiation and documentation. It contributes to ensuring studies progress through start-up toward site activation and compliance.

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Required Skills

SOPs
ICH/GCP
Regulatory Submissions
TMF
CTMS
Veeva Vault
Document Management
Communication
Detail-Oriented
Forecasting

+1 more

Qualifications

Bachelor's Degree in Life Sciences

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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