Scientist, Bioanalytical Contractor

Our Boston area client is seeking a contractor Bioanalytical Scientist to support assay development, validation, and sample analysis for RNA‑ and oligonucleotide‑based therapeutics. You’ll collaborate across research and in‑vivo teams, manage CRO assay transfer/validation, and ensure high‑quality data delivery. This role reports to the Senior Director of Bioanalytical. Scroll down to find an indepth overview of this job, and what is expected of candidates Make an application by clicking on the Apply button. Key Responsibilities Develop and validate assays to quantify oligonucleotides and protein biomarkers for ADME and pharmacology studies. Perform PK/PD and non‑clinical sample analysis; interpret and report data. Prepare method protocols and technical documentation. Present results in team and lab meetings. Support in‑vivo pharmacology and research teams. Manage CRO assay transfer, qualification/validation, and project tracking. Maintain accurate ELN records and support daily lab operations. Required Skills & Experience Bachelor’s (10+ yrs), Master’s (8+ yrs), or Ph.D. (2+ yrs) in a relevant field. Strong hands‑on experience with ligand‑binding assays (ELISA, MSD‑ECL). Experience with nucleic acid therapeutic bioanalysis (HELISA, H‑ECL) preferred. Solid understanding of assay development, validation, and ADME principles. LC‑MS experience is a plus. Familiarity with GLP, ICH, FDA guidance; regulated lab experience is a plus. Excellent problem‑solving, communication, and documentation skills. xywuqvp Proficiency with Word, Excel, PowerPoint, and GraphPad.