Clinical Research Associate

 Clinical Research Associate

[모집부서]
- Site Management in Pharmaceuticals

[업무개요]

1.      All aspects of site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites within the approved Clinical Development Plan (CDP).
2.    Incumbent is a key contributor of the clinical application with EC on behalf of Bayer Korea.
3.     Managing Investigator site and site activities and monitoring site data, to ensure patient safety and ethical and regulatory compliance necessary to provide quality data required for global regulatory submissions for approval of drugs including site study team management.
3.      Rigorous regulatory guidelines exist to ensure overall patient safety related to reporting of serious or unexpected adverse drug reactions.
4.       Incumbent is a key contributor in the preparation, conduct and follow up of Site Audits and Regulatory Inspections to ensure a successful outcome.

[자격요건]
The incumbent must have a Bachelor’s Degree (or equivalent) at least 2 years of monitoring & site management experience in oncology field. Pharmacist, nurse and related majors are preferred.

[우대사항]
- 보훈대상자