Medical Project Specialist
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate (Phase IV trials) at ICON supports the design and execution of post-approval and investigator-initiated clinical research across local, regional, and global settings. The role partners with internal and external stakeholders to advance Medical Scientific Affairs objectives while ensuring study quality, compliance, and stakeholder engagement. It contributes to ICON’s clinical development efforts and helps maintain strong site relationships.
Required Skills
- Project Management
- Budget Planning
- Site Feasibility
- IRB Submission
- GCP Knowledge
- Contract Negotiation
- Clinical Monitoring
- Audit Inspections
- Stakeholder Management
- Chinese
+1 more
Qualifications
- Bachelor's Degree in Life Sciences
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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