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.
Interested candidates who wish to apply for the advertised position, please click 'APPLY' to send in your resume.
EA License No: 13C6305
Reg. No.: R24120209
For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.
