Roles & Responsibilities
• Perform wet chemistry sample extraction as per study protocols and SOPs
• Handle centrifugation, evaporation, freezing, storage, and aliquoting of biological samples
• Prepare reagents, solvents, mobile phases, calibration standards, and QC samples
• Support method development and validation of drugs and metabolites using LC/MS/MS
• Execute validation parameters including accuracy, precision, recovery, matrix effect, and stability studies
• Carry out routine bioanalysis for bioequivalence and subject sample analysis
• Operate and maintain LC/MS/MS, HPLC, and ICP-OES instruments
• Perform system suitability checks, troubleshooting, and basic instrument maintenance
• Complete analytical worksheets, QC sheets, raw data records, and logbooks accurately
• Ensure compliance with GLP, SOPs, and regulated bioanalytical guidelines
• Support audits, inspections, and mandatory training activities
Qualification
• M.Pharm / M.Sc / MS (Science) – Any Specialization
Experience
• Hands-on exposure to LC/MS/MS bioanalysis preferred
• Experience with biological matrices such as plasma, serum, and urine is an advantage
• Regulated bioanalytical lab exposure is desirable (not mandatory)
Skills
• LC/MS/MS operation and troubleshooting
• Wet chemistry and bioanalytical workflows
• Bioanalytical method development and validation
• GLP compliance and documentation practices
• Data integrity and basic MS Office skills
About the Organisation
Cliantha Research is a leading global Contract Research Organization (CRO) providing integrated clinical research, bioanalytical, and regulatory services. The organization is known for its strong compliance culture, advanced analytical capabilities, and commitment to quality-driven clinical research.
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