This is a full-time hybrid role for a Clinical Research Coordinator with Client. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This role is located in Bengaluru but offers flexibility for some remote work.

• Experience with informed consent and developing protocols.

• Knowledge of research methodologies

• Clinical research experience and experience managing clinical trials.

• Excellent communication and organizational skills

• Attention to detail and ability to work independently.

• Bachelor's degree in a related field (e.g. life sciences, epidemiology)

• Experience working in a clinical research setting is a plus.