Clinical Research Coordinator
3 days ago
- Ensuring study entry criteria and informed consent procedures are fulfilled
- Coordination and Scheduling of visits to various sites
- Organize and participate in site initiation visit.
- Work in collaboration with study team to ensure trial preparedness.
- Play a role in developing and implementing recruitment plan to ensure long-term recruitment target is met.
- Monitors patients throughout the study to ensure study drugs are given accordingly and that protocols are followed.
- Collect, process and dispatch samples and other materials required by clinical trial protocols.
- Site liaison for Icon clinic staff, sponsor representatives, participants, investigators and external parties as required.
- Arranges for clinical and laboratory investigations to be carried out where appropriate. Ensure results of investigations and X-ray films are collected. Maintains records of additional investigations for invoicing purposes.
- Collects and collates research data, ensuring its accuracy and completeness.
- Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), or electronic CRFs.
- Requirements:At least 2-3 years' experience in clinical research or related healthcare experience
Invoicing
Administration
Data Entry
Compliance
Preparedness
Nursing
Life Sciences
Screening
Scheduling
Transcription
Laboratory
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