Senior Study Start Up Associate

Clinical Careers Page(2 days ago)

Chengdu, ChinaOnsiteFull TimeSenior$102,967 - $140,105 (estimated)Clinical Research

About this role

The Senior Study Start Up Associate at ICON plays a key role in supporting the initiation phase of clinical trials across countries. The position involves working within a dynamic team to ensure study start-up activities are conducted efficiently, with a focus on regulatory compliance, site identification, and patient safety.

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Required Skills

Feasibility
Regulatory Compliance
Site Identification
Contract Negotiation
Informed Consent
Clinical Trials
Study Start Up
Project Coordination
Patient Safety
Regulatory Submissions

Qualifications

Bachelor's degree or local equivalent
At least 3 years experience in clinical study start-up

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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