Clinical Research Associate Job Vacancy in Cavaxia clinical research academy Vijayawada, Andhra Pradesh – Updated today
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Company Name : Cavaxia clinical research academy
Location : Vijayawada, Andhra Pradesh
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Job Description : As a clinical research associate (CRA), you’ll run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe to allow on to the market. You’ll work on new and existing drugs and will usually be employed by either a pharmaceutical company or a contract research organisation (CRO), which works on behalf of pharmaceutical companies.You’ll 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.ResponsibilitiesTasks vary depending on your employer and level of experience. However, you’ll typically need to:develop and write trial protocols (outlining purpose and methodology)present trial protocols to a steering committeedesign data collection forms, known as case report forms (CRFs)coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjectsmanage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugsidentify and assess the suitability of facilities to use as the clinical trial siteidentify/select an investigator who will be responsible for conducting the trial at the trial siteliaise with doctors, consultants or investigators on conducting the trialset up the trial sites – ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)train the site staff to trial-specific industry standardsmonitor the trial throughout its duration, which involves visiting the trial sites regularlyverify that data entered onto the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)collect completed CRFs from hospitals and general practiceswrite visit reports and file and collate trial documentation and reportsensure all unused trial supplies are accounted forclose down trial sites on completion of the trialdiscuss results with a medical statistician, who writes technical trial reportsarchive study documentation and correspondenceprepare final reports and occasionally manuscripts for publication.Clinical Research Associate Requirements: Any life science graduates and the final year can apply.PGDiploma certification in Clinical Research1-2 Years of experience in the Clinical Research domain.Analytical mindset.Attention to detail.Exceptional interpersonal skills.Outstanding written and verbal communication.Excellent organizational skills.Willingness to continually self-educate.Job Types: Full-time, Regular / Permanent, FresherSalary: ₹15,000.00 – ₹20,000.00 per monthSchedule:Morning shift
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