Job Description
Job description
US Pharma MNC
Highlights- 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.
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