Job Descriptions

• To assist doctors to monitor the administration and progress of a clinical trial
• Oversee overall clinical operations related to the conduct of the clinical trial which includes recruitment of patients, ensuring study criteria are fulfilled, ensuring informed consent procedure is followed, visit coordination and scheduling
• Collect data from clinical trials
• Provide clinical trial support such as data entry and transcription. Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), or electronic CRFs
• Manage clinical trials through review, computerization, cleaning and auditing of clinical data and in compliance with standard operating procedures
• Validate clinical trial data to ensure consistency, integrity and accuracy
• Resolve queries on data inconsistencies
• Review case report forms for completeness and consistency
• Work in collaboration with study team to ensure trial preparedness

The Requirements

• Possess a Diploma/ Degree in Life Science or Nursing
• Ability to work both independently and in a team
• Good communication skills
• Meticulous and possess excellent organizational skills
• Computer literate