About BlueRock Therapeutics CELL+GENE™ platform , we direct cellular differentiation and apply precise genetic engineering to create transformative therapies for patients with serious neurological and ophthalmological diseases. Founded in 2016, BlueRock sits at the intersection of stem cell biology and genetic engineering. Our mission is to deliver authentic, functional cell therapies that address the root causes of disease—and to bring durable hope to patients with limited or no treatment options. What We Do Our foundational science enables the generation and directed differentiation of universal pluripotent stem cells into authentic, functional cells for allogeneic cell therapies. We are driven by scientific rigor, operational excellence, and an unwavering commitment to patients as we help shape the future of regenerative medicine. Our Neurology Vision BlueRock is advancing a differentiated pipeline of cell therapies in neurology focused on neurodegenerative and neurological disorders. Our lead program, bemdaneprocel (DA01) , is a first in class allogeneic cell therapy designed to replace lost dopaminergic neurons in Parkinson’s disease and is currently in Phase 3 development (exPDite2) across the U.S., Canada, and Australia. Our emerging neurology programs, including DA02 and MG0X , are in research stages and target additional high impact neurological conditions. Together, these programs reflect our ambition to restore function, slow or halt disease progression, and meaningfully transform standards of care. Our Ophthalmology Vision BlueRock is expanding its CELL+GENE™ platform into ophthalmology to address critical unmet needs in retinal disease. Our lead ophthalmology program, OpCT001 , is a first-in-class allogeneic cell therapy designed to replace damaged retinal pigment epithelial (RPE) cells in patients with advanced retinal disorders, including geographic atrophy secondary to age related macular degeneration. OpCT001 is currently being evaluated in a Phase 1 clinical study (CLARICO). Across all programs, BlueRock is committed to the highest standards of scientific excellence, ethics, compliance, and patient centric decision making, supported by a collaborative and inclusive culture. About the Role The Director, Program Management – DA02 will provide strategic and operational leadership for the DA02 neurology program as it advances toward IND submission and first in human clinical studies. This is a highly visible role that sits at the center of cross-functional execution, ensuring alignment to program strategy, timelines, resources, and enterprise objectives as this next generation cell therapy progresses. Reporting to the Vice President, Clinical Development – Neurology , this role partners closely with program and platform leaders to translate strategy into integrated, executable plans spanning CMC, nonclinical, clinical, regulatory, and supporting functions. The position is based at BlueRock’s headquarters in Cambridge, MA , with flexibility for a hybrid work model. The ideal candidate brings a strong foundation in scientific, technical, or operational roles within biopharma, coupled with deep experience in program leadership across IND enabling and early clinical development. Success in this role requires exceptional collaboration, clarity of communication, sound judgment, and a genuine passion for advancing innovative medicines to patients.
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Job Type
Full-time
Career Level
Director
Number of Employees
251-500 employees