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
Ensuring ICH GCP and Regulatory compliance is fundamental to the conduct of clinical research.
The objectives of this position are to plan, prepare, review and submit high quality Ethics Committee (IRB/IEC) and Health Authority applications to ensure timely clinical trial approval and start up for clients.
The position is based in our Bangkok office. As a member of our Regulatory Operations team you will be supporting submissions for project teams in Asia Pacific
• Graduate in a clinical, pharmacy or life sciences related field
• At least 2 years clinical research experience gained in a pharmaceutical company or CRO.
• Involvement in or exposure to preparation of Ethics Committee or Health Authority Applications in any country would be required.
• Involvement in study start up or in-house data review / monitoring and/or CRA experience would be advantageous.
• Training on Company processes and local country requirements would be available to ensure your success.
Interested applicants, please send your resume to: Ms. Thiranut
Email: thiranut.chankhot@ rsmthailand.com
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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