Research Executive

Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquartersin Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA),Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-endclinical research services to the global innovator, biotech, and generic pharmaceutical industries.

Act as a MV report writer for preparation of method validation report for small molecules and LBA based PK, PD and Immunogenicity assessment as per GLP non GLP regulatory guidelines

Prepare Method validation Reports for pk/pd/Immunogenicity Assays as per required GLP non GLP regulatory guidelines

Coordinate with operation team and compile relevant data required for preparation of MV Report

Coordinate with Quality control and Quality Assurance team for QC QA review of MV Report and resolve QC QA queries.

Ensure proper formatting and finalization of MV Report

Maintain track of method validation and manage MV report preparation to meet the timelines.

Prepare/update/maintain SOPs related to MV Report preparation.

02 or more years of MV Report writing experience in small molecules/ Biologics/ Biosimilar as per regulartory guidelines

MSc in Biotechnology/Biochemistry/Life Science