Mass General Brigham
Program Manager - Gene Editing & Therapy
Mass General Brigham, Boston, Massachusetts, us, 02298
Program Manager – Gene Editing & Therapy
Mass General Brigham
is seeking an experienced Program Manager to lead clinical and pre‑clinical gene editing and gene therapy projects.
The role combines clinical trial management, research coordination, and cross‑functional project leadership in a not‑for‑profit health system focused on patient care, research, and teaching.
Summary Manage multiple clinical research studies, supervise Clinical Research Coordinators, coordinate trial initiation and patient recruitment, develop standard operating procedures, advertise recruitment strategies, and oversee budgets and subcontracts.
Serve as liaison with sponsors, IRB, core laboratories, site PI’s, and study staff.
Key Responsibilities
Lead planning, execution, and oversight of preclinical gene editing and gene therapy projects.
Develop and maintain detailed project plans, milestones, resources, risk management, and budget tracking.
Coordinate with internal teams and external collaborators to design, implement, and analyze preclinical studies.
Serve as primary point of contact for communication between stakeholders, including scientific, operational, and regulatory teams.
Ensure preclinical studies comply with GLP, GCP, and 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/therapy and recommend innovative approaches.
Support business development efforts and represent the organization at conferences and partner meetings.
Qualifications
Bachelor’s degree in a related field (Master’s preferred).
5–7 years of research‑related experience required; 1–2 years of supervisory experience preferred.
Ph.D. in Gene Therapy, Molecular Biology, Genetics, or related life sciences; or equivalent industry experience.
Proven experience in pre‑clinical project management, especially in gene editing or gene therapy programs.
Hands‑on knowledge of molecular and cellular biology techniques, viral vector handling (AAV, lentivirus), and in‑vivo models.
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.
Strong organizational ability, attention to detail, and capability to prioritize tasks in a fast‑paced, innovation‑driven environment.
Location Boston, Massachusetts, United States (onsite or hybrid options may be considered).
EEO Statement Massachusetts Eye and Ear Infirmary is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law.
Applicants who require accommodation in the job application process may contact Human Resources at 857‑282‑7642.
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is seeking an experienced Program Manager to lead clinical and pre‑clinical gene editing and gene therapy projects.
The role combines clinical trial management, research coordination, and cross‑functional project leadership in a not‑for‑profit health system focused on patient care, research, and teaching.
Summary Manage multiple clinical research studies, supervise Clinical Research Coordinators, coordinate trial initiation and patient recruitment, develop standard operating procedures, advertise recruitment strategies, and oversee budgets and subcontracts.
Serve as liaison with sponsors, IRB, core laboratories, site PI’s, and study staff.
Key Responsibilities
Lead planning, execution, and oversight of preclinical gene editing and gene therapy projects.
Develop and maintain detailed project plans, milestones, resources, risk management, and budget tracking.
Coordinate with internal teams and external collaborators to design, implement, and analyze preclinical studies.
Serve as primary point of contact for communication between stakeholders, including scientific, operational, and regulatory teams.
Ensure preclinical studies comply with GLP, GCP, and 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/therapy and recommend innovative approaches.
Support business development efforts and represent the organization at conferences and partner meetings.
Qualifications
Bachelor’s degree in a related field (Master’s preferred).
5–7 years of research‑related experience required; 1–2 years of supervisory experience preferred.
Ph.D. in Gene Therapy, Molecular Biology, Genetics, or related life sciences; or equivalent industry experience.
Proven experience in pre‑clinical project management, especially in gene editing or gene therapy programs.
Hands‑on knowledge of molecular and cellular biology techniques, viral vector handling (AAV, lentivirus), and in‑vivo models.
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.
Strong organizational ability, attention to detail, and capability to prioritize tasks in a fast‑paced, innovation‑driven environment.
Location Boston, Massachusetts, United States (onsite or hybrid options may be considered).
EEO Statement Massachusetts Eye and Ear Infirmary is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law.
Applicants who require accommodation in the job application process may contact Human Resources at 857‑282‑7642.
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