Location: West (commonwealth area)
Working Hours: Office Hours ( 4-5 days a week)
NO EXPERIENCE NEEDED, TRAINING PROVIDED
Job Description:
- Set up and maintain study files and documents in both physical and electronic formats.
- Assist with preparing study-related materials and training documents.
- Enter, verify, and track clinical trial data to ensure accuracy and completeness.
- Prepare and organize documents for study reviews and monitoring visits.
- Support communication and coordination with the study team, vendors, and clinical staff.
- Receive and register clinical trial participants.
- Help process and prepare biological samples for testing and shipment.
- Monitor and manage inventory of study supplies and laboratory consumables.
- Assist in the maintenance and documentation of biomedical equipment and laboratory conditions.
Job Requirements:
- Min.
GCE O Level and above - Proficient in basic computer applications such as Microsoft Office
We are an equal opportunities employer.
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