Job Role Overview
You will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Working location: Client office, flexible work from home
Main Responsibilities:
* Site Monitoring and Management
* Oversee investigator sites throughout their lifecycle
* Work in accordance with ICH-GCP guidelines, study protocol, local and international regulatory requirements, and internal SOPs
Key Qualifications:
* Bachelor degree or higher qualification
* More than 2 years of site monitoring experience
* Oncology background required
* Native English speaker, excellent reading and writing skills
What We Offer:
We foster a diverse culture that rewards high performance and nurtures talent.
Competitive compensation package, including annual leave entitlements, health insurance, retirement planning, and employee assistance programme