Sample analysis using ligand binding assay, generate high quality bioanalytical data enable data summary and PK analysis.
Sample and reagent management using electronic tools including LIMS.
Fecal sample processing following environment health safety guidelines.
Plan and execute experiments based bioanalytical protocol and in vivo study design.
Analyze pre-clinical in vivo samples based on operational schedule.
Qualify ligand binding assay based on BA protocol, interpret result, and make decision on assay readiness.
Data archiving in ELN and LIMS.
Effectively communicate experimental plan, and results orally and in writing.
Contribute to technical report writing.
Sample management in LIMS.
Write, and update experimental protocols and procedures with supervision.
Initiate, design, interpret, troubleshoot operational assay independently and efficiently.
Bachelors Degree in biology, chemistry or pharmacology
0-2 years of pharmaceutical, biotechnology industry experience
Attention to detail
Ability to operate and maintain laboratory equipment with independence
Experience in automated ligand binding workflow is highly desirable
Experience in data driven troubleshooting ligand binding assay is highly desirable
Proven problem-solving ability
Excellent written and verbal communication skills and ability to draft technical reports
Proficiency with computers and data analysis software including Excel and LIMS
Ability to learn in face paced environment
Multi tasking ability
Lab Technical skills are preferred