General Clinical Research Officer
Job Description
Responsibilities
Conduct interviews, clinical measurements, and assist with assessments.
Collect health screening data accurately and confidentially.
Ensure participants understand study processes and consent appropriately.
Operate within SOPs, GCP, and ethical guidelines.
Work collaboratively with other CROs and study coordinators.
Job Requirement
Requirements
Diploma or Degree in Life Sciences, Nursing, Allied Health or related.
Prior experience in clinical trials or healthcare settings preferred.
Basic understanding of clinical research operations.
Work Hours: 6 hours/day (8:30am–3:30pm, incl. 1-hour break)
