Clinical Research Associate

Job Description

As a clinical research associate (CRA), youll run clinical trials to test new and existing drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use.Youll typically be involved in all stages of the clinical trial, including identifying an investigational site and setting up, initiating, monitoring and closing down the trial.Clinical trials may be carried out at various stages or phases and include trials on healthy humans, trials on patients with a disease, and studies conducted after the launch of a new drug to monitor safety and side effects. kindly send your update cv/resume to this email id ( hidden_email) for more details.ResponsibilitiesTasks vary depending on your employer and level of experience. However, youll typically need to:
• develop and write trial protocols (outlining purpose and methodology)
• 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

Keyskills :
clinical researchpharmaceutical careclinical neuropsychologyclinical psychologypediatric psychologyclinical pharmacologycritical care medicinemedical researchclinical data management