Study Co-ordinator

Main Responsibilities and Accountabilities

Follow and comply with clinical study guidelines, procedures and methodology as stipulated in individual study 

  1. Responsible for overseeing and coordinating the designated projects. 
  2. Able to manage online training modules 
  3. Good written and verbal communication skills in English and Malay 
  4. Obtain and file written consents from study participants 
  5. Able to organize time well and multitask 
  6. Handle cash reimbursement to study participants 
  7. Follow up with study participants as and when necessary 
  8. Maintain files and records of clinical studies for independent internal and external auditing 
  9. Order study materials, laboratory kits (if necessary) and other supplies for clinical studies 
  10. Able to extract data from source document and documents the information in the study records and CRF. 

Experience and Qualifications

At least a degree in a science field 

  1. Candidate must have 1 – 2 years’ experience in Research field 
  2. Experience as a project or study coordinator will be an added advantage 
  3. Experience in project implementation will be an added asset. 
  4. Experience in research data management. 
  5. Experience with RedCap data entry and management platform will be an added advantage. 
  6. Having completed the Good Clinical Practice (GCP) training and certification would be an additional advantage. 
  7. Knowledge and skills in molecular based laboratory techniques (optional) 


Always drives for results. 

  1. Must have innovative thinking skill; 
  2. Able to maintain high level of collaborative communications. 
  3. Able to commit to flexible working hours 

All interested candidate who meet the selection criteria may submit their application along with their details resume, to by 15th November 2022. 

All qualified applicants will receive consideration for employment. Only short-listed candidates shall be invited for interview. For further information, please contact, +603-22463383. 

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