Company Background :

Our client is leader of CRO business in Japan they offers tailored solutions for pharmaceutical companies, medical device manufacturers, academia, bio-ventures and medical institutions. 

Job Descriptions :

• Responsible for preparing and monitoring clinical trials by following the highest operation standards.
• Responsible in performing all monitoring aspects of clinical trials as stated in ICH E6 GCP/applicable local SOP/GCPs to assure all trials are conducted in strict adherence to good clinical practices, regulatory obligations, investigator integrity and compliance with project specific requirements. 
• Develop, compile and review all study-related regulatory and administrative documents from investigational sites, monitoring visit reports, work progression reports and other related documents.
• Support in feasibility studies, site and investigator identification as required.

Job Requirements :

• Applicants must have minimum Bachelor Degree in Nursing, Pharmacy or other science-related background.
• Applicants must have at least 4 years of experience in conducting clinical research or 2 years of direct experience as monitor in clinical studies.

Healthcare

Healthcare

Kuala Lumpur

Permanent

MYR 6,001 - MYR 8,000 / mth