Clinical Research Coordinator

Role & responsibilities

• Patient Recruitment and Screening: Identifying and screening eligible patients for clinical trials, ensuring they meet the study criteria.

• Informed Consent: Obtaining informed consent from participants, explaining the study's purpose, procedures, and potential risks.

• Data Collection and Documentation :Accurately collecting and documenting study data, including patient information, vital signs, and other relevant information.

• Protocol Adherence: Ensuring the study follows the established protocol, regulations, and ethical guidelines.

• Participant Monitoring: Continuously monitoring participant safety and well-being, reporting any adverse events.

• Communication and Coordination: Communicating with participants, investigators, and other team members to ensure effective collaboration.

• Administrative Tasks: Managing study budgets, supplies, and records.

Preferred candidate profile

• Graduation - B. Pharm
• Post-Graduation - M. Pharm
• Pharm D