The Analyst will be responsible for supporting bioanalytical studies within the clinical research domain, with a focus on method development, method validation, and routine sample analysis. The role requires strong technical expertise and adherence to established quality and regulatory standards.
The selected candidate will actively contribute to the execution of bioanalytical projects in full compliance with GLP (Good Laboratory Practices), GCP (Good Clinical Practices), and all applicable regulatory guidelines. The Analysts will additionally be responsible for providing supervisory support, guiding junior team members, and taking on broader project leadership responsibilities.
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