Clinical Research Coordinator
2 days ago
As a key member of our team, you will play a vital role in the coordination and execution of clinical trials. Your primary responsibility will be to ensure that all trial activities are conducted in accordance with International Conference on Harmonisation - Good Clinical Practice (ICH-GCP) guidelines and relevant regulatory requirements.
The ideal candidate for this position will possess excellent communication and organizational skills, with the ability to work effectively in a fast-paced environment. You will be responsible for maintaining essential documents, site files, and case report forms, as well as supporting the investigator in protocol compliance and patient coordination.
To succeed in this role, you should have a strong understanding of clinical research principles and procedures. Additionally, you should be highly motivated, with a keen sense of accountability and a commitment to delivering high-quality results.
Key Responsibilities:
- Coordinate clinical trial activities under supervision
- Maintain essential documents, site files, and case report forms
- Support the investigator in protocol compliance and patient coordination
- Ensure all trial activities adhere to ICH-GCP and ethical guidelines
- Participate in training sessions and team meetings as part of learning
Eligibility Criteria:
- Education: Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
- Experience: Fresh graduates only
- Strong communication and organizational skills
- Eagerness to learn and grow in the clinical research domain
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