Senior Molecular Laboratory Associate

We seek to hire a Senior Molecular Laboratory Associate for a direct hire job opportunity for our client in West Chicago, IL. Our client is a clinical metagenomics company focused on leveraging Next-Generation Sequencing technology against the most difficult infectious diseases. They utilize bespoke reagents, algorithms, and databases to give infectious disease physicians unprecedented insight into difficult cases. They target revolutionizing the manner and cadence of information delivery to clinical teams improving clinical outcomes and redefining how to diagnose infectious disease diagnostics.

This opportunity will focus on molecular diagnostic testing, clinical validation, and clinical reporting of metagenomic and PCR tests. The candidate must have prior experience in next-generation sequencing (NGS) library preparation, sequencing, and troubleshooting NGS workflows. To this end, the ideal candidate will have a rudimentary understanding of bioinformatic processes and manipulation of genomic data but bioinformatic work is not the focus of this position. The candidate must also have solid experience in the development of clinical protocols, validation of protocols, and delivery of laboratory-developed tests (LDTs).

The candidate will work closely with a team of diverse backgrounds and skills including members of the Research and Development, computational team as well as regular interaction with the Chief Medical Officer for guidance on experimental design, clinical validation, and reporting. A strong candidate will have the ability to work in a self-directed manner and manage direct reports when they are hired.

Education: 

• Achieved at least masters level training or bachelors with significant experience

Certifications: 

• ASCP Board of Certification (or equivalent) not necessary but a plus 

Prior Experience: 

• 1-3 years of industry or academic lab experience, specifically NGS library preparation
• Comprehensive documentation consistent with standards required by clinical regulatory authorities is required.
• Version control and documentation are critical skills needed for this position as some of the protocols being developed may be submitted to clinical regulatory bodies.

Other: 

• Excellent communication across local and remote teams is required
• Ability to regularly lift 25lbs
• Curiosity and careful attention to detail are required