Omega Therapeutics is a development-stage biotechnology company pioneering the first systematic approach to use mRNA therapeutics as a new class of programmable epigenetic medicines by leveraging its OMEGA Epigenomic Programming™ platform. The OMEGA™ platform harnesses the power of epigenetics, the mechanism that controls gene expression and every aspect of an organism's life from cell genesis, growth and differentiation to cell death. Using a suite of technologies, paired with Omega’s process of systemic, rational and integrative drug design, the OMEGA platform enables control of fundamental epigenetic processes to correct the root cause of disease by returning aberrant gene expression to a normal range without altering native nucleic acid sequences. Omega’s engineered, modular, and programmable mRNA-encoded epigenetic medicines, Omega Epigenomic Controllers™, target specific intervention points amongst the thousands of mapped and validated proprietary and novel DNA-sequence-based epigenomic loci, EpiZips™ to durably tune single or multiple genes to treat and cure disease through Precision Genomic Control™. Omega is currently advancing a broad pipeline of development candidates spanning a range of disease areas, including oncology, regenerative medicine, multigenic diseases including immunology, and select monogenic diseases.
About the Role:
Omega Therapeutics, Inc. is seeking a Study Coordinator to join our Early Development team. The successful candidate must be a scientifically motivated self-starter, capable of working with minimal supervision and is enthusiastic, detail oriented with a passion for bringing novel medicines to patients and comfortable working on a fast-paced scientific team.
Work with Study Directors/Sponsors in study design, protocol preparation, and overseeing conduct of studies if needed
Effectively manage multiple tasks/projects simultaneously to meet internal/external deadlines while maintaining organizational integration within the Discovery and Early Development team
Work seamlessly with project teams to plan, resource and prioritize outsourced academic collaborators and with contract research organizations
Demonstrated experience in delivering high quality nonclinical safety and DMPK data packages for drug candidate selection and beyond
Excellent organizational and time-management skills including the ability to manage several projects simultaneously
Outstanding teamwork, communication, and interpersonal skills
B.S. or M.S in the biologic or safety sciences, 3-5 years industry experience
Strong scientific writing skills
Experience in preparing regulatory submissions (e.g. IND)