The average salary for a Clinical Research Associate (CRA) is $66,315. What do Clinical Research Associates do? A clinical research associate (CRA) is a health care or life sciences professional who oversees clinical trials on behalf of pharmaceutical companies, medical research institutes and government agencies. Typical employers of clinical research associates include pharmaceutical companies and clinical contract agencies. Their job description entails monitoring clinical trials, working directly with the sponsor company as an independent freelancer or for a contract research organization. These programs can be completed in two years and can be offered through both the online and the hybrid formats. CRAs often go by various titles, including clinical research coordinators, clinical program managers, clinical research administrators, and clinical trial associates. The role of a CRA can vary between different companies. The job description will be the same. Visit PayScale to research clinical research associate (cra) salaries by city, experience, skill, employer and more. A clinical research associate is a healthcare professional who performs many activities related to medical research and clinical trials. The title will vary from company to company. A Clinical Research Associate’s experience requirements are necessary to prove their expertise in the profession. The amount of studies and number of sites allocated to a CRA will depend on the complexity of the trial. Clinical Research Associate (CRAs) are responsible for coordinating and overseeing the execution of studies and clinical trials. For example, you may find associate degree programs. Now that we explained that potentially confusing aspect of the job, let’s jump right into the question of what this job actually entails. According to the Association of Clinical Research Professionals (ACRP) a Clinical Research Associate (CRA) is: A CRA supervises, monitors, and supports the administration and progress of a clinical trial on behalf of a sponsor. Typical employers | Qualifications and training | Key skills Clinical research associates help to organise and monitor the different phases of clinical trials of drugs. Typically, a CRA will set up, monitor and close-down clinical studies, which is what I do. For example, a senior clinical research associate requires skills like cra, site management, clinical … This field is taken as a certificate program course in many schools. Senior clinical research associates and study coordinators both require similar skills like investigator meetings, clinical trials, and crf. What does a Clinical Research Associate do? Key responsibilities include: What does a clinical research associate do? Take their skills, for example. Analyzes and evaluates clinical data gathered during research. A Clinical Research Associate (CRA) can also be called a Monitor, a Clinical Monitor, a Trial Monitor or a Medical Monitor. A Clinical Research Associate participates in the design, administration and monitoring of clinical trials. Clinical trials are the method by which new pharmaceuticals and medicinal treatments are developed, and clinical research associates are an integral part of that process. The role of the clinical research associate is to ensure that medical devices, new treatments and new drugs are approved for patients' use.. They have a hand in everything from recruiting study participants to creating study documentation, collecting patient data, and performing quality assurance audits to ensure study protocols are being followed. While some skills are similar, others aren't. 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