Our client is a Leading Asia Pacific Contract Research Organization (CRO), Clinical Trials (Phase I to IV clinical research), Biostatistics, Data Management, Regulatory Affairs, Audits, Medical Writing, and Commercialization - across all major therapeutic areas
The core focus of the CRA role is to ensure the rights and the wellbeing of the trial participants are protected and the reported trial data is accurate, complete and verifiable from source documents. The CRA is also the primary link between Investigational sites and Sponsor, acting as a site manager ensuring that clinical trials are conducted and documented as per ICH GCP guidelines, global and local regulatory requirements and Company/Client SOP’s.
• Tertiary qualifications in clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered)
• At least 2-3 years of independent CRA experience
• Solid knowledge of GCP, national and international regulations and a sound understanding of how they apply to you
• Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments
• Previous experience in monitoring oncology trials would be highly desirable
• A strong track record of performing visits to sites according to the Clinical Monitoring Plan.
Interested applicants, please send your resume to: Ms. Thiranut
For more information, please call 02-670-9020 ext. 167
Interested applicants, please send your application letter with resume indicating qualifications, expected salary and a recent photograph to:
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