Cliantha Research Jobs in India

The MD/MV group develops and validates assay methods for drug analysis in biological fluids using LC/MS/MS. · Evaluate precision accuracy stability of drug/metabolite in biological fluid after extraction. · ...

The Clinical Trials QA Specialist will be responsible for planning and execution of day-to-day quality assurance activities, delegation/allocation of work to quality assurance auditors, and planning of Investigator site audits in consultation with CT operation team. · ...

Role & responsibilities · Responsible for screening of the subjects in the trial and monitor the day to day activities of the study team. · To monitor vitals and adverse events during the study · Preferred candidate profile · MBBS with registration is mandatory · ...

The Business Development Manager will identify potential clients, promote services offered by Cliantha research Ltd, · and represent the company at conferences. · ...

A medical writer prepares protocols and documents as per regulatory requirements in consultation with group members. · ...

Role & responsibilities · Study Related Activities: · - Perform method development, method validation, and study sample analysis for immunoassays, ligand binding assays, or other large molecule assays under the supervision of Project Manager(s). · - Perform ELISA and other ligand ...

This is an overview of the QA auditor position. · Planning and execution of day-to-day quality assurance activities · Delegation/allocation of work to quality assurance auditors · ...

The GCC QA role is responsible for coordinating and maintaining Global GxP compliance programs and centralized QMS, including SOP governance, metrics, risk management, and inspection readiness. This role partners with cross-functional stakeholders to harmonize processes, respond ...

Medical monitor · PRINCIPAL DUTIES AND RESPONSIBILITIES: · Note: These statements reflect the general description of the position and are not intended to be an all-inclusive list of tasks to which the employee may be assigned. · A. Provide medical input in the protocol design, me ...

The incumbent will be responsible for method development validation and routine bioanalysis of drugs and their metabolites in biological matrices using LC/MS/MS. · Perform sample extraction using wet chemistry techniques as per study protocols and SOPs. · Handle centrifugation ev ...

This is a contract manager position in Ahmedabad. · Initiation of Feasibility with internal technical team after thoroughly reviewing the new inquiry · Follow-up and tracking of feasibility from internal technical team · ...

Role & responsibilities: · Strategic HR Planning · Talent Acquisition and Onboarding · Employee Relations · HR Compliance and Regulatory requirements and other legal compliances · Employee Engagement and Retention · ...