Project Manager for Editing and Gene Therapy Preclinical Studies

Position Overview

We are seeking an experienced Project Manager to lead and coordinate preclinical research programs in
Gene Editing and Gene Therapy
for genetic hearing loss. The ideal candidate will oversee cross-functional teams, manage collaborations with external partners (CROs, academic institutions, and biotech companies), and ensure timely and compliant execution of preclinical projects that support early therapeutic development.

• Lead planning, execution, and oversight of preclinical gene editing and gene therapy projects, ensuring alignment with program objectives and timelines.
• Develop and maintain detailed project plans, including goals, milestones, resource, risk management, and budget tracking.
• Coordinate with internal teams and external collaborators to design, implement, and analyze preclinical studies, including molecular, cellular, and in vivo experiments.
• Serve as the primary point of contact for communication between stakeholders, including scientific, operational, and regulatory teams.
• Ensure preclinical studies comply with GLP, GCP, and relevant regulatory standards.
• Prepare and review study protocols, reports, and other scientific documentation for internal and external submission.
• Facilitate decision-making by providing data-driven insights, risk assessments, and project status updates.
• Monitor technological trends in gene editing/gene therapy and recommend innovative approaches to enhance project outcomes.
• Support business development efforts, including discussions with potential collaborators and partners.
• Represent the company at conferences, scientific presentations, and partner meetings as needed.

• Ph.D. in Gene Therapy, Molecular Biology, Genetics, Biochemistry, Immunology, or related life sciences; or equivalent experience in industry.
• Proven experience in
  Preclinical Project Management
  , particularly in gene editing (e.g., CRISPR, ARCUS) or gene therapy programs.
• Hands‑on knowledge of molecular and cellular biology techniques, viral vector handling (AAV, Lentivirus), and in vivo models preferred.
• Demonstrated ability to manage cross‑functional teams and multiple projects simultaneously.
• Experience with contracting and coordinating work with CROs and external collaborators.
• Familiarity with regulatory requirements for preclinical studies supporting Investigational New Drug (IND) applications.
• Strong analytical, problem‑solving, and decision‑making skills.
• Excellent verbal and written communication skills, including scientific reporting and stakeholder presentations.
• Proficient in project management software, Microsoft Office Suite, and data analysis tools.
• Ability to work independently while fostering collaboration within multidisciplinary teams.

• Strong organizational ability, attention to detail, and capability to prioritize tasks in a fast‑paced, innovation‑driven environment.
• Proactive, self‑motivated, and adaptable, with willingness to "roll up sleeves" and support experimental work as needed.
• Excellent interpersonal skills, diplomacy, and cultural sensitivity to manage international collaboration.
• Passion for advancing gene therapy and precision medicine to benefit patients.

Boston, Massachusetts, United States.