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 [redacted].
Additional EEO Contact Information
California Relay Service: [redacted] (TTY), [redacted] (Voice) TTY is a Telecommunications Device for the Deaf and is reachable only from phones equipped with a TTY Device.
