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$38.5K

$102.7K

$162K

How much do project manager gene cell therapy jobs pay per year?

As of Jun 11, 2026, the average yearly pay for project manager gene cell therapy in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Project Manager in Gene Cell Therapy, and why are they important?

To thrive as a Project Manager in Gene Cell Therapy, you need a solid background in life sciences or biomedical engineering, project management expertise, and often a relevant advanced degree or PMP certification. Familiarity with regulatory requirements (such as FDA, EMA), project management tools like MS Project, and laboratory information management systems (LIMS) is highly valued. Exceptional organizational skills, leadership, and the ability to communicate complex scientific concepts clearly are crucial soft skills. These competencies ensure successful coordination of cross-functional teams, compliance with stringent regulations, and effective delivery of innovative gene and cell therapy projects.

What are Project Manager Gene Cell Therapy?

A Project Manager in Gene Cell Therapy oversees the planning, execution, and completion of projects related to gene and cell therapy research and development. They coordinate cross-functional teams, manage budgets and timelines, and ensure compliance with regulatory requirements. Their role is crucial in guiding therapies from early-stage research through clinical trials to commercialization, ensuring that milestones are met efficiently and effectively. Project Managers also serve as the main communication link between stakeholders, including scientists, regulatory bodies, and executive leadership.

What is the difference between Project Manager Gene Cell Therapy vs Clinical Research Coordinator?

AspectProject Manager Gene Cell TherapyClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, project management certification often preferredBachelor's in health sciences or related field, clinical research certification beneficial
Work EnvironmentBiotech or pharmaceutical labs, clinical trial sites, project teamsHospitals, clinics, research sites, clinical trial settings
Industry UsageUsed in biotech, pharma, and gene therapy companies for project oversightCommon in clinical research organizations and hospitals for trial coordination

The Project Manager Gene Cell Therapy focuses on overseeing gene therapy projects, managing timelines, budgets, and teams. In contrast, the Clinical Research Coordinator handles the day-to-day operations of clinical trials, ensuring protocol adherence and patient safety. While both roles require knowledge of clinical processes, the Project Manager has a broader project oversight role, whereas the Coordinator is more involved in trial execution.

What are some typical challenges a Project Manager faces when coordinating cross-functional teams in gene and cell therapy projects?

Project Managers in gene and cell therapy often navigate complex challenges such as aligning diverse scientific, regulatory, and clinical teams. These projects require managing timelines and resources across departments like R&D, quality assurance, and manufacturing, each with distinct priorities and technical languages. Effective communication and adaptability are key to resolving conflicts, ensuring milestones are met, and maintaining compliance with stringent regulatory standards. The role is highly collaborative, and success often depends on building strong relationships and fostering a culture of transparency within multidisciplinary teams.
Infographic showing various Project Manager Gene Cell Therapy job openings in the United States as of June 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Senior Scientist, Cell Therapy Process Development

GeneFab

Alameda, CA • On-site

$140K - $175K/yr

Full-time

Posted 14 days ago

Job description

GeneFab is seeking a highly skilled Senior Scientist to join our Cell Therapy Process Development team in Alameda, CA. In this role, you will lead the design and optimization of integrated processes, bridging the gap between innovative synthetic biology and phase-appropriate cGMP manufacturing. If you have hands-on experience with automated cell processing and a passion for driving clinical readiness for next-generation genetic medicines, we want to hear from you.
Responsibilities:
  • Design and perform experiments to optimize integrated processes for cell therapy, including: evaluation of cell sources, isolation and activation of human immune cells, media optimization, viral/non-viral genetic modification, cell expansion, cell harvest/fill/finish, and cryopreservation.

  • Cell therapy process scaleup, including: transition from open processes to closed automated systems, understanding analytical methods, using a Design of Experiments (DoE) approach, and evaluating process choices within a Quality by Design (QbD) framework

  • Exploration of new technologies or materials for process scale-up or improvements with quality mindset leading to clinical or commercial readiness.

  • Cross-functional collaborations in project teams to translate scientific understanding to development of phase appropriate cGMP cell therapy manufacturing unit operations.

  • Lead the design, execution, and analysis of experimental studies for new manufacturing technologies and processes

  • Author and review study protocols, technical reports, ELNs, regulatory submissions.

  • Support authoring of key documentation to enable technology transfer (e.g. sampling plans, batch records, specifications, SOPs, FMEA, flow diagrams, etc.).

  • Help coordinate sample management workflow across Process and Analytical Development teams and manage development database

  • Serve as a technical resource/SME for GMP operations (e.g. root cause analyses and continuous improvement initiatives)

  • Coordinate and prioritize tasks across multiple projects

  • Maintain familiarity with current state-of-the-art related to cell therapy processes

Qualifications:
  • BS/MS with 6+ years or PhD with 4+ years of experience in science/engineering of biopharmaceutical or cell/gene therapy process development and technology transfer

  • Hands-on experience with automated cell processing units or platforms (i.e. bioreactors, automated cell wash, fill and finish) is critical.

  • Experience developing and optimizing cell therapy processes for GMP production with quality mindset

  • Strong technical writing and communication skills to support both development and tech transfer applications

  • Strong critical thinking, organizational skills, ability to work in multi-functional project teams, and attention to detail

  • Experience with various types of cell therapy products (i.e. CAR-T, CAR-NK, HSC, MSC) is preferred

  • Experience with AI solutions for CGT processes and working with LIMS is a plus

$140,000 - $175,000 a year
About GeneFab
GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies.
We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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