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Principal Clinical Data Standards Consultant
ICON Clinical Research
Opportunity Description
China-Principal Clinical Data Standards Consultant
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Principal Clinical Data Standards Consultant at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your focus will be on coordinating consulting and advisory services delivery, resolving issues, and developing team capability.
Key responsibilities include:
+ As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for:
+ Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
+ Collaborating with cross-functional teams...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Principal Clinical Data Standards Consultant at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your focus will be on coordinating consulting and advisory services delivery, resolving issues, and developing team capability.
Key responsibilities include:
+ As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for:
+ Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
+ Collaborating with cross-functional teams...
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