Clinical Trial Associate

Our client, a Global award-winning surgical robotics company

Responsibilities:

• To arrange and support the setup of clinical/pre-clinical trials
• To collect documents and data from clinical trial information in accordance with the applicable Good Clinical Practice (GCP) guidelines for clinical studies
• To identify the needs, bottlenecks and deviation found during the studies
• To participate in research and development projects when request
• To take on other the tasks and contribute to the optimisation of the processes within the corporate
• To prepare and completed the ethical and regulatory approval processes
• To design and perform preliminary tests to the clinical/pre-clinical studies;
• To record the experiments/tests/studies/trial results and generate the associated reports for internal use and for regulatory approval processes

Requirements: 

• To jobholder possesses a bachelor’s degree or above in biomedical engineering, medicine, medical/life sciences, or related disciplines
• Min 2-3 years experience in clinical studies or trial management 
• Good knowledge of Good Clinical Practice (GCP) and regulations of clinical trials are necessary.
• Candidates with experience in medical devices development or associated research/clinical studies preferred
• Good communication skills of written and spoken English and Chinese;

Interested parties, please send the CV to "Apply To Position"/ cv@aral.com.hk.

***Personal data collected will be used for recruitment purposes only***

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