Job Description

Responsibilities:

• Plan and execute experiments based on bioanalytical protocol and in vivo study design.
• Analyze pre-clinical in vivo samples based on operational schedule.
• Qualify ligand binding assay based on bioanalysis 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 and day-to-day lab operations.
• Sample management and sample data QC in LIMS.
• Write and update experimental protocols and procedures.
• Initiate, design, interpret, troubleshoot operational assay independently and efficiently.

Requirements:

• BS or MS degree in biology, chemistry, or pharmacology.
• 3+ years of pharmaceutical and/or biotechnology industry experience.
• Attention to detail, experience performing lab testing, independent, and self-motivated.
• Ability to properly use common lab tools such as pipettes.
• Ability to operate and maintain laboratory equipment independently.
• Experience with lab automation is highly desirable.
• Must Have Experience with ligand binding workflow is required.-(MSD Experience)
• Experience in data driven troubleshooting 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 and willingness to work effectively in a highly collaborative and multidisciplinary environment.

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