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.

• 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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