Job Description

The Singapore Eye Research Institute (SERI) is seeking a highly qualified individual to join our team to conduct innovative and world-leading basic science, clinical and translational eye and vision research.

He/ She will be expected to, but not limited to:

Assist the investigators to recruit, screen, and follow-up on participants of the study, in strict adherence to the study protocol, Singapore Good Clinical Practice (GCP) Guidelines, and other applicable regulatory and ethical requirements

Perform study procedures on study participants (consent taking, administrative duties, ocular imaging-related tests, etc.)

Handle entry and validation of study data, extraction of relevant information from medical records, reporting of adverse events, maintenance of investigator files, and other essential documentation

Coordinate scheduling and conduct of clinical trials with hospital procedures for study participants as well as related finances and logistics

Attend clinics to recruit potential study participants for clinical studies

Maintain certification for GCP, local regulatory, and protocol compliance

Support in other functions such as general administration or coordination as required by the studies

Participate in the housekeeping of SERI Research Clinic as well as her activities

Job Requirements

At least Diploma in Optometry, Nursing, or Sciences related studies from a recognised tertiary institution

Training will be provided. Relevant experience in clinical trials/IRB and training in GCP is an advantage.

Ability to manage multiple projects simultaneously and effectively work in teams and independently

Possess excellent interpersonal and communication skills, meticulous, diligent and keen to work in a multi-team setting. Opportunity to be based off-site i.e., different sites for recruitment of research participants