Clinical Research Associate

As a Clinical Trials Assistant, you will play a crucial role in supporting various aspects of clinical trials. Your responsibilities will include assisting in site selection, initiation, monitoring, and close-out visits for clinical trials to ensure their successful implementation. It will be your responsibility to ensure that all clinical trials are conducted in compliance with the protocol, ICH-GCP guidelines, and regulatory requirements. You will be tasked with maintaining accurate and proper documentation of all trial activities and reporting findings effectively. Your role will also involve supporting data verification by meticulously comparing source data with Case Report Forms (CRFs). Effective communication with investigators and site staff will be essential to address and resolve any issues that may arise during the trials. In addition, you will be expected to assist in tracking project timelines and deliverables to ensure the smooth progression of the trials. It will also be necessary for you to attend training sessions regularly to stay updated with the latest regulatory guidelines and industry standards. This is a full-time, permanent position suitable for freshers who are looking to kickstart their career in the field of clinical trials. The benefits of this position include health insurance, paid sick time, and Provident Fund. The work location for this role is in person, providing you with a hands-on experience in the clinical trials environment.,