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 Qualifications
BCA,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 Details
Sallary-35K To 58K
Experience:-0 To 4 Years
Minimum Age-18+
Working hours-8 Hour
Work Department-Medical Coding,Billing,Clinical Research Associate
Work Industry-Pharma,Healthcare
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HR TEAM
Keyskills: billing patient assessment healthcare coding patient care