Blog

Designation:

• – Clinical Research Associate

Job Description:

• – On-Site Review of Method Development Data and associated procedures
• – On-Site Review of Method Validation Data and associated procedures
• – On-Site monitoring of the Bioanalytical Phase
• – Incurred Samples Reanalysis, Repeats and Batch Failures
• – Investigations during the bioanalytical phase
• – Preparation of Monitoring Checklist and Report
• – Key role in associating with the Head of the Department for the Continuous Improvement Program
• – Closely work with Project Managers
• – Addressing and fulfilling client requirements
• – Actively participating in new initiatives
• – Training new joiners
• – Able to Perform monitoring based on sponsor expectations
• – Extensive Travelling would be pre-requisite for this role
• – Management of Personal Training Records

Basic Requirements:

• – Frequent travelling
• – Good Communication skills
• – Have a strong hold on email communications
• – Should hold a Master’s Degree in Pharmacy or Science
• – Should be able to travel abroad

Note*

• – Make sure to send your CV mentioning the JOB CODE