Associate Clinical Research Coordinator,Investigational Medicine Unit (Contract)

You will work in an early phase research environment that facilitates clinical research studies, academic and educational activities. You will provide research support service in clinical trials and ensure the delivery of trial-related services complies with regulatory guidelines, i.e. International Conference on Harmonization-Good Clinical Practice (ICH-GCP).

You will be involved in project management, performing trial related duties, laboratory and/or medical procedures, in accordance to requirements and conditions stipulated by trial protocol or as assigned at the Principal Investigator’s (PI) professional discretion.

Job Requirements:

• Diploma in Life Sciences/Pharmaceutical Sciences/Clinical Trials Management
• Preferably with 2 years’ relevant experience in clinical research coordination and at least 1-year phlebotomy experience
• Preferably attended theInternational Conference on Harmonization-Good Clinical Practice (ICH-GCP)Programmeor equivalent
• Preferably attended and attained competency certification for Venepuncture
• Proficiency with MS Word and Excel
• Meticulous and possesses good interpersonal skills
• Team-player, proactive and able to work in a fast-paced environment

We regret that only shortlisted candidates will be contacted.