Position: Clinical Research Coordinator


Clinical Operation Co-ordination

  • Act as a coordinator between Investigators and Sponsors/ CRO in clinical trials.
  • Planning, starting up and executing clinical trials within allocated resources, budget and timeline.
  • Liaise with trial subjects on their schedule visit in clinic.
  • Provide administrative and clinical supports to Investigators.
  • Proper documentation of trial reports and data.
  • Processing, packing and arranging shipments for clinical trial bio samples.
  • Accountability and handling of investigational products.
  • Reporting of AEs/ SAEs to Sponsor.
  • Submit required documents and safety reports to Ethics Committee.
  • Assist in maintaining clinical department equipment and facility.
  • Adhere to Good Clinical Practice and regulatory policy.


  • Possess Bachelor’s Degree in Science such as Pharmacy, Pharmacology, Biomedical, Nursing, Medical Science or equivalent. Fresh graduates are welcome to apply.
  • Good interpersonal and communication skill.
  • Good written and spoken in English, Malay and Chinese language. Able to communicate in local dialects is an advantage.
  • Hardworking, organised, meticulous and willing to learn.
  • Detailed and good analytical and problem solving skills.
  • Good team players.
  • Able to work according to the clinical research study schedules and adapt well in hospital environment.
  • Able to handle blood, urine and other clinical samples.
  • General computer skills include Microsoft Word, Excel and PowerPoint.
  • Have own transportation and willing to travel.