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Added 10 hours ago
Portfolio & Program Management Associate
Vertex Pharmaceuticals Incorporated
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The Associate Director (AD) of Portfolio and Program Management (PPM) sits within the COO's organization at Vertex and leads programs from Research through early Development. This role will…
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Research Scientist/Engineer Senior
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The Associate Director (AD) of Portfolio and Program Management (PPM) sits within the COO’s organization at Vertex and leads programs from Research through early Development. This role will…
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- $70 to $90 USD / hour
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experience. At The Tauri Group, we do what’s right for the Program, the
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Discovery IT Co-op (Spring 2027)
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Scientific Marketing Manager / Director – Biologics Discovery and Development
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Senior Scientist/Engineer (Regenerative Medicine & Advanced Biological Systems)
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Added 5 days ago
Portfolio & Program Management Director
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Closed listing

CIRM

Senior Science Officer, Clinical Development

South San Francisco, CA, United States

$154,891 to $213,704 USD / year

This opening has closed.

The original listing is kept below for reference.

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Job details

Pay: $154,891 to $213,704 USD / year
Experience: Doctorate (PhD, PharmD, MD/DO,) in medicine, biomedical research or a related area with 5 years or more of work experience in a science-related discipline beyond doctoral degree.
Posting language: English
Posted: Oct 27, 2026

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Original job description

Archived listing. The details below describe a past opening.

Background

The California Institute for Regenerative Medicine (CIRM) is a state agency created by California voters to accelerate stem cell and gene therapies for people with unmet medical needs. Since 2004, Californians have entrusted CIRM with $8.5 billion to accelerate promising discoveries through clinical trials, train a regenerative medicine workforce, strengthen the state’s biotechnology economy, and expand access to transformative treatments. Today, CIRM is pioneering new models of therapy development and accelerating medical breakthroughs that change lives - in California and around the world. For more information, visit www.cirm.ca.gov.

General Statement

The mission of the Clinical Development Team is to attract and support the most innovative and high-quality stem cell and genetic therapy-based clinical projects for CIRM funding. We aim to advance cutting-edge science and drive transformative breakthroughs in regenerative medicine. Our primary goals include supporting and accelerating the clinical and pre-commercial development of regenerative medicine therapies from first-in-human studies to readiness for submission of marketing approval applications. To support clinical development of stem cell and genetic therapy-based therapies, CIRM also supports critical research infrastructure such as the CIRM Alpha Clinics Network.

Role Summary:

The Senior Science Officer, Clinical Development, will help manage a portfolio of clinical trial project awards, will provide clinical operations subject matter expertise across all relevant CIRM programs and will interface with the Patient Access Team for Clinical Infrastructure support. In this role, the Senior Science Officer will work cross-functionally with the Clinical Development, Preclinical Development, Patient Access, Grants Management and Review Teams within CIRM.

The Senior Science Officer will have expertise and experience in a scientific research discipline, preferably one that relates to stem cells, cell and gene therapies, or drug or device preclinical and clinical development. The Senior Science Officer will have extensive experience in the design and operation of clinical trials.

The Senior Science Officer will have an innate sense of urgency and determination to deliver outstanding results and to find innovative ways of meaningfully advancing CIRM's mission.

Job Functions

Overseeing a Portfolio of Clinical Trial Stage Awards

Working in a team environment in advancing the most promising clinical stage stem cell-based and genetic therapies for unmet medical needs.
Managing the development of project milestones and contracting of awarded clinical trial stage projects.
Monitoring the programmatic, scientific and/or technical progress of an awarded clinical trial stage project, supporting milestone achievement in a timely manner.
Assessing the progress of projects through objective metrics and ensuring complete and up-to-date reporting on all projects in your portfolio.
Working with the project teams to proactively identify risks or deficiencies with active projects and leveraging internal and external resources to ensure success.
Leveraging internal and external resources to ensure success, or recommend appropriate action to suspend/discontinue projects when warranted.
Seeking new and innovative ways to improve and accelerate the therapies through clinical development.
Monitoring resources to ensure they are being used appropriately and efficiently.
Working with CIRM colleagues to support a highly competitive review process to ensure only the most promising and well-constructed projects are considered for inclusion in the Clinical Development portfolio.

Leveraging CIRM Clinical Infrastructure to Support Clinical Development Projects

Working collaboratively with CIRM Patient Access Team to increase patient access to CIRM-funded therapies.
Working collaboratively with CIRM Patient Access Team to leverage CIRM Clinical Infrastructure Programs for accelerating clinical development of CIRM-funded therapies.

Building, Advancing, and Communicating the Portfolio

Being up to date on trends and key developments in the stem cell and gene therapy research field.
Seeking new and innovative ways to improve on the conduct of science.
Helping to connect scientists with potential collaborators, resources or programs that would advance an important scientific project or direction.
Providing consultations with potential applicants to address questions about the applications process.
Collecting data and helping to track progress across CIRM-funded portfolios to inform priorities and alignment of ongoing and future funding opportunities; creating and maintaining slides for reporting portfolio to different stakeholders and CIRM leadership.
Contributing to the planning and organization of CIRM-sponsored webinars, scientific workshops and grantee/trainee conferences.
Supporting the development and implementation of new funding programs or improvements to existing funding programs in partnership with the team lead and internal stakeholders.
Representing CIRM at appropriate scientific, medical, governmental, and industry meetings and events.
Engaging with all stakeholders (scientific thought leaders, subject matter experts, patient advocacy groups) to build support for and advance projects.
Working with colleagues to promote, support, and disseminate information about the Clinical Development team and related activities to the public and other stakeholders, as appropriate.

Harmonizing with the CIRM Mission

Demonstrating commitment to CIRM’s mission in your words and actions.
Collaborating with others to generate efficiencies, enhance productivity, and develop competencies.
Developing and organizing internal guidance and SOP documents for CIRM processes in collaboration with other CIRM teams.
Showing commitment to team decisions by supporting and working to achieve team objectives.

Qualifications (Experience and Education)

Doctorate (PhD, PharmD, MD/DO,) in medicine, biomedical research or a related area with 5 years or more of work experience in a science-related discipline beyond doctoral degree.
Three years of demonstrated management experience in leading preclinical development, clinical development and/or manufacturing of stem cell-based therapies or genetic therapies.

Desirable Skills and Abilities

Strong knowledge of drug development, manufacturing process, clinical operations and regulatory for stem cell-based therapies and genetic therapies.
Proven track record in leading cross-team collaboration to deliver high-quality outcomes.
Ability to effectively manage, organize and prioritize multiple projects and meet deadlines in a fast-paced and demanding environment.
Outstanding communication skills.
Ability to work collaboratively in a team environment.
Ability to make clear, concise and impactful presentations.
Ability to embrace change and a desire to learn.

Working Conditions

Hybrid environment, required to work 2 days in the South San Francisco office and three days remotely. In-person attendance of organizational meetings and board, subcommittee, and working group meetings as required.
Prolonged periods of sitting at a desk and working on a computer.
Must be willing to work in a high-rise building.
Ability to operate standard office equipment.
Be available to work outside of normal business hours.

Supervision Received

The Senior Science Officer reports to the Senior Director of Clinical Development.

Supervision Exercised

None

Compensation

This position is expected to pay $154,891 - $178,416 annually, which fits within the full salary range of $154,891 - $213,704 annually, for the Program Manager job classification. It is uncommon for an individual to be offered a salary close to the upper end of the full range for a position. Salary for this position will reflect the final candidate’s qualifications, experience, skills, knowledge, relevant education, and certifications, in addition to being aligned with the internal leadership peer group.

Benefits

https://benefits.calhr.ca.gov/state-employees/

Required Application Documents

Applicants must submit a resume and cover letter to be considered for this position.

Applicants requiring reasonable accommodations for the interview process should inform the interview scheduler at the time of scheduling.

For general questions regarding this position or inquiries specifically related to reasonable accommodations or Equal Employment Opportunity (EEO), please contact jobs@cirm.ca.gov.

Additional EEO Contact Information

California Relay Service: 1-800-735-2929 (TTY), 1-800-735-2922 (Voice) TTY is a Telecommunications Device for the Deaf and is reachable only from phones equipped with a TTY Device.

Equal Opportunity Employer

The State of California is an equal opportunity employer to all, regardless of age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (includes pregnancy, childbirth, breastfeeding and related medical conditions), and sexual orientation.

About employer

More about this job

Skills

Clinical trials
Microsoft Access
Research
Stem cells
Work as a team
Reporting
Leadership
Circulate information
Collaboration
Manufacturing processes
Meet deadlines
Communication skills
Presentation skills
Office equipment

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