USV Pvt. Ltd Released Job Openings On 27/05/2022.USV Pvt. Ltd is an Indian multinational pharmaceutical and biotechnology company in Mumbai, India. The company operates across 75 countries globally, and is a leading producer of Metformin in India. The company was founded by Vithal Balkrishna Gandhi to provide affordable and quality healthcare to every Indian..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for USV Pvt. Ltd Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.Â
Vacancy Details:
USV Pvt. Ltd Recruiting M.Pharma Candidates with 00-01+ Years of Experience for Clinical Researcher (R & D) Departments.Complete Details for the Clinical Researcher (R & D) Departments as follows.
Important Details :
- Location :Mumbai (All Areas)( Govandi )
- No of Vacancies: 01
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application:27/05/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : Icon Clinical Research Released Work From Home Job Opportunity
Job Description/Skills Required
- Review of bioavailability and bioequivalence clinical study protocols, Literature search, relevant study documents such as CRF, ICF etc and Clinical study report (eCTD) including appendices.
- Review of bioanalytical method validation and bioanalytical reports.
- Co-ordinate with the internal team for getting the documents for DCGI BE NOC application.
- IMP shipment to CROs after obtaining the EC and or BE NOC approval before the study initiation.
- Meticulous planning and tracking of the clinical trial and clinical studies and deliverable as per the defined timeline of regulatory submission.
- Monitoring of clinical trial and bioequivalence studies at various CROs/clinical sites viz subject enrollment as per inclusion and exclusion criteria, compliance of study conditions as per approved protocol, study drug dosing, Biological sample analysis, Adverse event management and reporting if occurred etc.
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