Doctor
cliantha research ltd · Ahmedabad · onsite · Posted 49d ago
Undisclosed1–2 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Role & responsibilities
-
Efficiently planning and executing the logistics of all clinical studies.
- Responsible for overall conduct of the bioavailability bioequivalence clinical studies under supervision.
- Responsible for selection of the participants in the trial, safety of the subjects, operation of the clinic, communication with the sponsor, ethics committee and study team.
- Responsible for screening of the participants in the trial and monitor the day to day activities of the study team.
Job Location: Ahmedabad
Required Qualifications/ Experience:
- MBBS degree from a recognized institution
- Valid Medical Registration Certificate
- 1-2 years of experience in conducting and managing Bioavailability (BA) and Bioequivalence (BE) studies.
Sourced from naukri
Skills
clinical researchclinical trialsICH-GCPClinical OperationsbioequivalenceBioequivalence Studies
About Cliantha Research

cliantha research ltd
Clinical Research
894
employees
2004
22 years old
Ahmedabad, Gujrat
India
₹4.8L PA avg
Avg at Cliantha Research
About
Cliantha Research is a Clinical Research Organization offering comprehensive services aimed at ensuring regulatory compliance in clinical trials across various therapeutic areas.
Industries
Clinical ResearchBiotech & Life sciencesAnalytics & KPO
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