APDM Pharmaceuticals Private Limited has its office in Ahmedabad with all QA and regulatory support staffs for managing CDO and CDMO projects ,vendor Audits, BA BA monitoring, project and Engg team. We are a global pharmaceutical service providers with a vast global network of CMO’s, CDMO’s and CRO’s. We have more than 100 years of CDMO, 50 years of R&D and decades of regulatory and QA experience in our company. We have proved ourselves as reputed, reliable and value added service providers to Pharmaceutical Industries in USA, UK, EMEA, Canada and other PICS countries..
Post : Clinical Research Associate (BE Monitoring / CT Monitoring)
Qualification - MPHARM (Pharmacology) 3 to 6 years
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
• Able to Perform monitoring based on sponsor expectations
Address : 403 Patron Building, Rajpath Rangoli Road, Behind Rajpath Club, Satellite, Ahmedabad 380054, Gujarat
Interested candidates share their resume with subject mentioned for post applied Hr@apdmpharma.com
Last Date : 15th June, 2023
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