Clinical Research Associate

Job Description

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 Research Associate Responsibilities:identify/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 on a regular basis and dealing with and solving any issuesverify that data entered on to 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 reportsEducational QualificationsBCA,MCA,Bsc.IT,Msc.IT,IT,Diploma,B.Tech,M.Tech.Bachelors degree in biological science or a related field.Skills-Knowledge of the pharmaceutical industry, terminology, and practices.Other DetailsSallary-35K To 58KExperience:-0 To 4 YearsMinimum Age-18Working hours-8 HourWork Department-Medical Coding,Billing,Clinical Research AssociateWork Industry-Pharma,HealthcareIf you want to join this job, call the number given below-hidden_mobileAlso Send Your CV-Best RegardsHR TEAM

Keyskills :
codingpatient assessmentbillingpatient care