Clinical Research Associate (CRA)/ Sr. CRA

Clinical Research Associate (CRA) will be responsible for running clinical trials to test drugs for their effectiveness, risks, and benefits, ensuring that these drugs are safe to be released on the market. CRAs typically are involved in all stages of the clinical trial, including identifying an investigational site and setting up, initiating, monitoring, and closing down the trial.• Develop and write trial protocols.• Present trial protocols to a steering committee.• Design data collection forms, known as case report forms (CRFs)• Coordinate with the ethics committee, which safeguards the rights, safety, and well-being of all trial subjects.• Manage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs.• Identify and assess the suitability of facilities to use as the clinical trial site.• Identify/select an investigator who will be responsible for conducting the trial at the trial site.• Liaise with doctors, consultants, or investigators on conducting the trial.• Set up the trial sites.• Train the site staff to trial-specific industry standards.• Monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis.• Verify that data entered onto the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)