Cliantha Research Limited – Walk-In Interviews for M.Sc / B.Pharm / M.Pharm on 27th May’ 2023 - Jobplacementhub

Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL. Cliantha Research is headquartered in India with facilities in Ahmedabad, Noida and Vadodara.

We are conducting walk-in interviews for following..!!!

Position:Research Scientist

Qualification: M.Sc / B.Pharm / M.Pharm

Experience: 1 to 6 yrs

Salary: 2-5 Lacs P.A.

Location: Ahmedabad

Time and Venue:

27 May , 2.00 PM – 5.00 PM

3rd Floor, Commerce House II, Opp. Pushparaj Tower, Judges Bungalows Road, Bodakdev, Ahmedabad – 380054, INDIA

Report Specialist

Roles and Responsibilities:-

A. Prepare Sample analysis report and Method validation report in compliance with standard operating procedure.

B. Ensure report is prepared as per respective regulatory and sponsor requirement.   

C. Handle Sponsors or regulatory queries on lab reports.

D. To ensure that lab reports are released within their timelines.

E. Maintain documents and databases for the assigned projects.

F. Compile copies of Method validation report and Sample analysis report for archiving.

Report Viewer

Roles and Responsibilities:-

A. To ensure that the data is entered in a timely fashion to meet deadlines.

B. To ensure 100% validation data review for the completeness of documentation and in compliance with all applicable standard operating procedures and regulation.

C. Ensure quality and integrity of data.

D. Maintain documents and databases for the assigned projects.

E. Ensure the completeness of documentation pertaining to a method validation.

F. Report to the Study Director/R&D supervisor for method validation related any deviations.

G. Review of Analytical Laboratory system for GLP Compliances.

H. Compile method validation for archiving.

I. Ensure reconciliation of forms after completion of method validation.

J. Preparation of summary tables of Method validation.

K. To assist Project manager/Analyst for preparation of Analytical procedure.

L. Responsible for all activities of Lab archivist in absence of Lab Archivist or as and when require.