We are seeking a Clinical Trial Coordinator (CTC) to join our team. In this role, you will be an integral part of the clinical research process, ensuring that our trials are conducted in accordance with all regulatory requirements and that the integrity of the data is maintained.
Key Responsibilities:
- Coordinate and manage clinical trials from start to finish.
- Ensure compliance with all regulatory requirements.
- Assist with the preparation of study protocols, consent forms, and other trial-related documents.
- Maintain accurate and up-to-date trial documentation.
- Communicate effectively with study sponsors, clinical research associates, and other stakeholders.
- Monitor trial progress and report any issues or deviations.
- Assist with data collection, analysis, and reporting.
Qualifications:
- Bachelor’s degree in a scientific or health-related field.
- Previous experience in clinical research or related field is preferred.
- Strong organizational and communication skills.
- Attention to detail and ability to manage multiple tasks.
- Proficiency in Microsoft Office Suite.
- Ability to work independently and as part of a team.
Why Join Us:
- Opportunity to work with a leading global CRO.
- Be a part of a team dedicated to improving global health.
- Fully remote work with flexible hours.
- Career growth and development opportunities.
