Clinical Research Associate - Oncology
Top 10 Global Pharmaceutical Company.
Global level studies.
About Our Client
My client is one of the top pharmaceutical companies with good reputation. They dedicate themselves to multiple disease areas. Also, they provide many disease areas trials and good internal training to develop their employees. Currently, they are looking for experienced CRAs to join their team and develop together.
Responsible for site monitoring, site management activities and close-out visits, and ensure regulatory, ICH-GCP and protocol compliance.
Assess factors that might affect safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
Understand project scope, budgets, and timeline; besides, manage site-level activities/ communication to ensure project objectives, deliverable and timeline are met.
Provide input into study documentation and monitoring worksheets.
Develop effective relationship with investigator site staff to ensure that key clinical metrics are met.
The Successful Applicant
Master degree or equivalent in a health care or other scientific disciplines.
2 years above site monitoring experience.
Comprehensive knowledge of GCP/ICH guidelines and relevant regulations.
Good documentation/ communication skills.
Good command of English and Chinese.
What's on Offer
- Competitive salary package.
- Proactive and transparent internal culture.