0 - 4 years
0 Lacs
Posted:1 week ago|
Platform:
On-site
Full Time
We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials. The clinical research associate will manage multiple aspects of the subjects' welfare. You will conduct regular site visits, generate and distribute internal and external newsletters, prepare final reports, and liaise with interested parties regarding all trial aspects.
Responsibilities
Creating and writing trial protocols, and presenting these to the steering committee.Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial.Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.Ordering, tracking, and managing IP and trial materials.Overseeing and documenting IP dispensing inventory, and reconciliation.Protecting subjects confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.
Other Details
Salary-49,000/- to 65,000/-Required Experience-0 To 4 YearsMinimum Age-18
Requirements
Qualification Required-Bsc,Msc,Ssc,Diploma,Bachelors degree in biological science or a related field.Work Department-BillingWork Industry-IT,Automation,Banking,Finance,Education,Telecom,Pharma,MedicalSkills-Working knowledge of medical terminology and anatomy.
for more clarification contact to this number-9211083197
Also Share Your CV -harsheeta.hs1987@gmail.com
Regards
HR Placement Team
DEVIKA STAFFING SOLUTION
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