LIMs Data Associate

LIMs Data Associate – Discovery Life Sciences

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Discovery Life Sciences is a leading provider of highly characterized human biospecimens and cellular starting materials to advance cell and gene therapy and precision medicine programs for cancer, infectious disease, and other complex conditions. We routinely manage hundreds of studies and expertly test thousands of biospecimens simultaneously. Leading biopharma, diagnostic and academic institutions trust us to quickly deliver high‑quality biospecimens and reliable, reproducible biomarker data, so they can outpace their competition and push the leading edge of innovation using our Science at your Service TM business model.

The LIMs Data Associate assists in reviewing/analyzing data and documentation and supports quality checks, LIMS troubleshooting, data transfer, and documentation management within our biopharma environment.

• Conduct quality checks for clinical and non‑clinical project work.
• Troubleshoot LIMS system and collaborate with quality team for LIMS modifications.
• Transfer clinical trial data and handle new project setup paperwork.

• Bachelor’s degree.
• 2+ years of relevant industry experience required.
• Experience with Labware LIMS is a plus.
• Meticulous attention to detail, strong computer and multi‑tasking skills required.
• Excellent verbal and written communication skills.
• Team‑oriented with ability to work across functional departments.

• Receive and maintain delivered data logically and organized, troubleshoot repair and compile files for efficient utilization of trial data.
• Assist in producing, analyzing, updating, and maintaining data procedural documentation.
• Document new procedures and functions into data management practices, ensuring up‑to‑date and accurate documentation.
• Prioritize and manage data transfer to keep production flow on schedule.
• Perform quality control checks, verify study and report data against documentation, notify inconsistencies, file QC documentation.
• Work within a laboratory information management system (LIMS) for setup of new studies.
• Identify and resolve quality issues with study teams and Report Writing teams.
• Review sponsor deliverables and verify study records at intervals.
• Ensure study data is complete, current, and stored appropriately, enforce project standards.
• Adhere to Health and Safety regulations, security procedures and company policies.
• Respect privacy of personal patient information and coworkers.

Base pay $24–$32 per hour (location based). Benefits include medical, dental, vision, life insurance, disability coverage, 401(k) match, paid time off, professional development, inclusive environment, team events.

IN OFFICE – Newtown, PA. Applications accepted until the role has been filled.

Equal Opportunity Employer. Veterans and individuals with disabilities encouraged to apply.

• Associate
• Full‑time
• Science