Singapore | Posted: Nov 26, 2024

General Responsibilities

• Demonstrates professional and clinical excellence in the care and management of clinical trial subjects/volunteers in the CRU.

• Respect subject/volunteers' privacy and keeps in strictest confidence all privileged information.

• Collects, verifies and ensures proper storage of data collected.

• Be proficient in the operation of biomedical equipment within the CRU.

• Applies standard safety precautions to protect self and others from biohazard materials including blood borne pathogens.

• Participate actively in Code-blue drills and lead in the event of a real emergency.

General Screening

• Performs general screening activities.

Clinical Trial Related Activities

• Performs protocol related tasks as assigned by the Study Nurse-in-Charge.

• Ensures clinical trial procedures/t...