CTA - Bulgaria / Poland
Clinical Careers Page(2 months ago)
About this role
A Clinical Trial Associate at ICON supports clinical research activities within a global CRO, contributing to the conduct and quality of clinical studies. The role is based in Bulgaria or Poland and helps ensure accurate study documentation and compliance with regulatory standards to advance investigational treatments.
Required Skills
- Clinical Trials
- Trial Documentation
- Regulatory Compliance
- Informed Consent
- Case Report Forms
- Metrics Reporting
- Stakeholder Communication
- Organization
- Detail Oriented
Qualifications
- Bachelor's Degree in Scientific or Healthcare Field
About Clinical Careers Page
iconplc.comICON 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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