Clinical Process Development Associate III, Product Development Team

Broad Institute
United States, Massachusetts, Burlington
Apr 17, 2025
Description & Requirements We are seeking an experienced and motivated Clinical Process Development Associate III to join Broad Clinical Lab's Product Development Team. In this role, you will contribute to the design, execution and interpretation of experiments intended to explore novel multiomics technologies. The ideal candidate has hands-on experience with molecular biology techniques and a strong curiosity to develop and apply novel methods in a multi-disciplinary team-based environment. CHARACTERISTIC RESPONSIBILITIES INCLUDE Collaborate with molecular biologists, computational scientists and leadership to support the feasibility exploration and development of next generation sequencing (NGS) products. Contribute to the design and execution of process development experiments. Perform data analysis interpretation and troubleshooting of novel high-sensitivity duplex and multiomics sequencing approaches. Establish performance specifications for NGS products and partner with application scientists and leadership to establish proof-of-concept data sets for novel approaches. Author detailed, accurate, and accessible records of experimental data and protocols, assay validation plans and reports within a quality management system. Present scientific and technical data to colleagues in a clear and cohesive manner. Work collaboratively with sequencing vendors and development partners to bring cutting-edge new technologies into BCL. QUALIFICATIONS/ SKILLS BS, MS, or Ph D in a scientific or engineering discipline 5 years of relevant experience, preferably in a clinical or research genomics laboratory environment Strong hands-on experience with next-generation sequencing workflows, automation platforms, and molecular biology techniques Advanced experimental design and data interpretation skills, including a familiarity with bioinformatics tools and systems for statistical data analysis (Excel, JMP, R) Demonstrated experience working under regulated environments (CLIA or quality system) Excellent scientific writing and presentation skills