Responsibilities:

l  Manage day-to-day operational aspects of assigned projects including third-party vendor activities.

l  Act as CRA (Clinical Research Associate) during the operation phase of clinical trial. Responsible for the timely and accurate completion of project documentation, such as protocols, amendments, case report forms and study report, stored appropriately and audit-ready.

l  Communicate with investigators. Ensure quality and adherence to GCP. Ensure investigators to follow required training and to complete the required documentation timely.

l  Report the progress of clinical trial on regular basis. Maintain close working relationship with sponsors to achieve client satisfaction, operational and customer service excellence.

l  Provide high quality assistance to support clinical trials according to applicable regulatory requirements and SOPs within budget and timelines.

l  Provide nutritional insight during the planning phase of clinical trial

l  Other duties and assignments as requested for the overall performance of the clinical team.

Qualifications:

l  Master degree in nutrition, public health and food science, or related scientific fields. Biochemistry and human/animal physiology are mandatory. Oversea education is a plus.

l  Ability to prioritize multiple tasks, plan proactively and accomplish goals using well defined instructions and procedures in a fast-paced environment

l  Capable to work in full English environment. CET-6 pass is minimum.

l  Strong attention to detail, and meticulous follow-through.

l  Strong team spirit in order to successfully work with cross-function and cross-nation teams.

l  Ability to travel up to 10%% of time of job related responsibilities.