US Pharma MNC

• West Area (Nearest MRT: Buona Vista/Commonwealth/One-North)
• 2 shift duties (AM & PM)
• Flexi Arrangements for Locums

• 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.