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.
- Stay updated on relevant regulations, guidelines, and industry best practices in clinical research.
Requirements
- Bachelor's degree or above in Life Sciences, Pharmacy, or a related field.
- Prior experience as a clinical research associate or in a similar role.
- Knowledge of clinical trial processes and regulatory requirements.
- Good understanding of Good Clinical Practice (GCP) guidelines.
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
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