Highlights :
- West Area (Nearest MRT : Buona Vista / Commonwealth / One-North)
- Office Hours (must be comfortable to cover Afternoon Shifts during high peak period)
- Flexible - can plot your own schedule
- Must attend a 4-day paid training
Job Description :
Screen study participants in accordance with regulatory guidelines and ethical standards.Conduct informed consent discussions and ensure participants understand the study's requirements.Monitor patient progress and collect data during clinical trials, ensuring accurate documentation.Administer study-related interventions as per protocol, including medications and treatments.Conduct assessments and follow-ups with participants, addressing any concerns and providing education.Maintain accurate records and databases, and assist with data analysis as needed.Participate in training sessions and workshops to stay updated on clinical research practices.Requirement :
Valid SNB & BCLS requiredDiploma / Degree in NursingAble to start Dec'25 onwardsAble to perform IV Cannulation and PhlebotomyOpen to take without research experience, on the job training provided!
Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button
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