Clinical Research Associate (CRA)

The responsibilities for this position include monitoring clinical trials to ensure adherence to protocols and regulations, conducting site visits to verify data accuracy and compliance, assisting in patient recruitment and ensuring informed consent procedures, maintaining trial documentation, reporting findings to stakeholders, and ensuring proper handling and storage of investigational drugs. Additionally, collaborating with investigators, sponsors, and regulatory authorities is a key aspect of this role. Key skills required for this position include attention to detail to ensure accuracy in trial data and documentation, regulatory knowledge with an understanding of GCP, FDA, and ICH guidelines, effective communication skills for interaction with research teams and sponsors, problem-solving abilities to address challenges in trial execution, and project management skills for coordinating multiple aspects of clinical studies. This is a full-time position with benefits such as health insurance and Provident Fund offered. The work schedule is during day shifts and the work location is in person.,