Infoclin Consultancy

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