Clinical Research Coordinator

Role Overview: As a Clinical Research Coordinator (CRC), you will be responsible for managing and coordinating the day-to-day operations of a clinical trial. This includes tasks such as recruiting and screening participants, obtaining informed consent, collecting and managing data, and ensuring compliance with study protocols and regulations. Additionally, you will act as a liaison with sponsors, investigators, and regulatory bodies, maintain meticulous records, and may perform basic clinical procedures. Key Responsibilities: - Manage and coordinate the day-to-day operations of a clinical trial - Recruit and screen participants - Obtain informed consent from participants - Collect and manage data effectively - Ensure compliance with study protocols and regulations - Act as a liaison with sponsors, investigators, and regulatory bodies - Maintain detailed and accurate records - Perform basic clinical procedures as required Qualifications Required: - Bachelor's degree in a relevant field (e.g. life sciences, healthcare) - Strong organizational and communication skills - Attention to detail and ability to maintain accurate records - Knowledge of clinical trial processes and regulations is preferred Please note that the company provides benefits such as a flexible schedule, food provision, health insurance, paid sick time, and Provident Fund. The work location for this role is in person. (Note: Any additional details of the company were not present in the provided job description),