Clinical Research Associate
- Aashtha Staffing
- 98 Positions
- 3 months ago
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Job Description
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 Research Associate Responsibilities:
identify/select an investigator who will be responsible for conducting the trial at the trial site
liaise with doctors, consultants or investigators on conducting the trial
set 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 standards
monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis and dealing with and solving any issues
verify 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 practices
write visit reports and file and collate trial documentation and reports
Educational Qualifications
BCA,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 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
Employement Category:
Employement Type: Full timeIndustry: Medical / HealthcareRole Category: Medical TranscriptionFunctional Area: Not SpecifiedRole/Responsibilies: Clinical Research AssociateContact Details:
Company: Aashtha StaffingLocation(s): Aurangabad,
Keyskills: accounting transmission coding medical billing healthcare
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