
Clinical Research Assistant/ Administrative
2 weeks ago
**Responsibilities**:
- Assist in the planning and execution of clinical research studies.
- Coordinate and oversee the collection, analysis, and interpretation of study data.
- Ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Conduct site visits to monitor study progress and ensure adherence to study procedures.
- Manage study documentation, including case report forms and informed consent documents.
- Collaborate with study investigators and study team members to ensure smooth study operations.
- Conduct training sessions for study site personnel on study procedures and requirements.
- Prepare study reports and contribute to the development of study protocols and study-related documents.
**Requirements**:
- Degree in Optometry, Life Sciences, Pharmacy, or equivalent.
- At least 5 - 8 years of clinical research experience with ophthalmology background.
- Prior knowledge of clinical trial processes and regulatory requirements.
EA License No: 13C6305
Reg. No.: R24120209
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