Clinical Research Specialist

Role Overview: You will be responsible for developing and reviewing study protocols and informed consent documents. Monitoring clinical trial progress and ensuring adherence to GCP, FDA, and IRB regulations will be a key part of your role. You will also be involved in collecting, managing, and analyzing clinical data, preparing regulatory submissions and study reports, as well as collaborating with cross-functional teams including investigators and coordinators. Key Responsibilities: - Develop and review study protocols and informed consent documents - Monitor clinical trial progress and ensure adherence to GCP, FDA, and IRB regulations - Collect, manage, and analyze clinical data - Prepare regulatory submissions and study reports - Collaborate with cross-functional teams including investigators and coordinators Qualifications Required: - Prior experience in clinical research or related field - Knowledge of GCP, FDA, and IRB regulations - Strong attention to detail and organizational skills - Excellent communication and teamwork abilities Please note that the job type for this position is full-time and open to fresher candidates. The work schedule is during the day shift and the work location is in person. Additionally, the company provides health insurance benefits. Role Overview: You will be responsible for developing and reviewing study protocols and informed consent documents. Monitoring clinical trial progress and ensuring adherence to GCP, FDA, and IRB regulations will be a key part of your role. You will also be involved in collecting, managing, and analyzing clinical data, preparing regulatory submissions and study reports, as well as collaborating with cross-functional teams including investigators and coordinators. Key Responsibilities: - Develop and review study protocols and informed consent documents - Monitor clinical trial progress and ensure adherence to GCP, FDA, and IRB regulations - Collect, manage, and analyze clinical data - Prepare regulatory submissions and study reports - Collaborate with cross-functional teams including investigators and coordinators Qualifications Required: - Prior experience in clinical research or related field - Knowledge of GCP, FDA, and IRB regulations - Strong attention to detail and organizational skills - Excellent communication and teamwork abilities Please note that the job type for this position is full-time and open to fresher candidates. The work schedule is during the day shift and the work location is in person. Additionally, the company provides health insurance benefits.