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You will be updated with latest job alerts via emailMedical Investigator Vimta Labs Ltd Cherlapally
Qualification: MBBS
CTC: As per market standards
Looking candidates from Clinical Research Organization only.
Primary Responsibilities:
that Good Clinical Practices (GCP) are followed.
planned studies as per protocol requirements quality system procedures and SOPs.
of pre study health records.
written informed consent before each Volunteer participation in the trial.
that clinical data is complete accurate and is recorded as per protocol and SOP requirements.
and documentation of UDS reports & additional test reports.
of eligibility status.
of daily Temperature log Urotherm reading Emergency medication kit documentation and expired medication discarding.
research staff on conducting the trail and Group briefing of ICF to volunteers
SAE management reporting and documentation.
the trial throughout its duration.
the data entered on to the CRFs is consistent with source data.
maintenance including management of emergency conditions.
of Vitals documentation ECG Phlebotomy and Xray procedures.
of X ray films and X ray report destruction.
study reports assessments and documentation.
status of CRFs and documentation.
Secondary Responsibilities:
of ICFs CRFs.
and Evaluation of Volunteers for study participation.
of drug administration to volunteers.
Interested candidates can share their resumes to .
Required Experience:
Junior IC
Full-Time