Clinical Research Coordinator

In this role, you will be responsible for coordinating and overseeing clinical trials to ensure smooth operations. Your key responsibilities will include: - Recruiting and screening study participants, while ensuring informed consent is obtained. - Maintaining accurate records of study activities and participant data. - Communicating effectively with investigators, sponsors, and regulatory authorities. Your qualifications should include: - Strong organizational and communication skills. - Knowledge of GCP and regulatory guidelines. - Attention to detail and the ability to multitask. - Proficiency in data management and software. The job type for this position is full-time, and the benefits include health insurance and provident fund. The work schedule is during day shifts, and the work location is in person.,