Hiring For Clinical Research Associate

Job Description

You will be required to manage the data collected during trials, oversee trial sites, and conduct regular site visits to monitor the progress. You will also collaborate with the sponsors at trial sites and ensure the tests are conducted ethically while adhering to applicable regulations and guidelines.Clinical Research Associate Responsibilities:Reviewing and approving study-related documents, such as informed consent forms.Conducting source data verification and ensuring data quality.Managing trial supplies and drug accountability.Serving as a liaison between study sites, sponsors and regulatory agencies.Educational QualificationsBCA,MCA,Bsc.IT,Msc.IT,IT,Diploma,B.Tech,M.Tech.Bachelors degree in biological science or a related field.Skills-Strong attention to detail and accuracy in data management.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 :
healthcarepatient carecodingbilling