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. You will play a leading role in generating and overseeing documentation and records.
Clinical Research Associate 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-30,000/- to 50,000/-
Required Experience-0 To 10
Minimum Age-18
Requirements
Qualification Required-Diploma,B.tech,M.tech,
Bachelors degree in biological science or a related field.
0 To 4 years of industry experience also can apply
Work Department-Clinical Research Associate
Work Industry-Pharmaceutical
Skills-Available to travel extensively and on short notice, and ability to manage travel schedules,
for more clarification contact to this number-9821543366
Also Send Your CV
[email protected]
Regards
HR Placement Team
This job is provided by Shine.com
