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Location:
Ho Chi Minh City, Ho Chi Minh City, Vietnam
Job reference: R-037403
Posted date: Dec. 12, 2018
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1/ Management of the Clinical Research Projects

·         Set and monitor appropriate standards and timelines for clinical & data management processes according to the sponsoring company (MC/TA) standards.

·         Review all company protocols, reports and manuscripts to ensure that they meet scientific objectives

·         Ensure all clinical trials comply to GCP/AstraZeneca Quality Standards.

·         Track resource utilisation and trial performance to ensure maximum efficiency

·         Ensure clinical research objectives are communicated effectively to the local research team

·         Ensure AZ/GCP standards are met in projects outsourced to CROs

2/ Process Management & Development

·         Develop and implement a quality enhancement program

·         Develop initiatives which increase the efficiency and effectiveness of the clinical trial process

·         Implement international directives on process changes

3/ External Liaison and Image

·         Participation/representation on scientific boards, relevant professional meetings and committees

·         Attend relevant local and international research meetings and conferences

·         Develop and maintain close contact with TA clinical groups

·         Develop and maintain network of academic/professional contacts to act as key participants in clinical trials

.         Contribute to image of AstraZeneca through further education & training including literature review

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Clinical Research Associate
Clinical Development

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