
Clinical Research Coordinator
2 weeks ago
You will support and assist the Principal Investigator in the following trial related activities:
- Patient screening and recruitment,
- Monitoring subject's compliance to their treatment and follow-up,
- Data collection and management including resolving data discrepancies,
- Coordinating the collection of biological specimens,
- Monitoring of adverse events and safety reporting,
- Maintaining and organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities,
- Tracking of trial expenditures and timely invoicing.
Requirements:
- Degree in Life Sciences/Nursing
- OR Diploma in Nursing with minimum 6 years working experience as CRC
- 2 years of related working experience will be advantageous
- Excellent time-management and communication skills
- Able to work independently and as a team
- Detail-oriented and self-motivated
- Good grasp of MS Office applications
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