Research Associate

Coordinate and participate in clinical research studies, including collection, compilation, documentation, and analysis of clinical research data, and perform regulatory processes across multiple studies.

Requirements

• Able to work accurately and with minimal supervision.
• Ability to comprehend written instructions given by the related departmental personnel.
• Ability to plan & organize ones work schedule effectively.
• Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel.
• Affinity to work in team.
• Enthusiasm.