Clinical Research Coordinator (Dept of Reproductive Medicine, 2-year contract)

To work closely with the Principal Investigator (PI) to conduct and coordinate research related activities and projects. The incumbent is also responsible for the organisation of the research data and other ad-hoc duties as assigned by the Principal Investigator.

• Provide administrative support to the research project; coordinate and organise research data and/or files, as well as monitor and study data;
• Assist in recruiting subjects, obtaining informed consent from subjects, scheduling subjects for protocol visits and following-up on subjects; and
• Any other adhoc duties as assigned

Job Requirements:

• Candidate must possess at least Bachelor Degree in Life Sciences or related disciplines;
• At least 1 Year of working experience in the related field and healthcare industry;
• Possess knowledge in Good Clinical Practice;
• Strong writing, presentation, communication and interpersonal skills; and
• Independent, dynamic and self-motivated person who is able to work independently as well as in a team.