Fate Therapeutics Inc. Jobs Hiring Now
Fate Therapeutics Inc. is hiring for 6 open roles on Migrate Mate as of July 15, 2026, concentrated in nursing and procurement & supply chain, with listed salaries up to about $310,000. Migrate Mate updates Fate Therapeutics Inc.'s live openings daily. Fate Therapeutics is a clinical-stage biopharmaceutical company focused on developing programmed cellular immunotherapies for patients with cancer.
Find Fate Therapeutics Inc. JobsOverview
Fate Therapeutics Inc. hiring data on Migrate Mate, as of July 15, 2026.
- Open jobs
- 6
- Top team
- Nursing
- Seniority
- Manager level or above
- Work type
- 0% remote or hybrid
- Top location
- San Diego
- Salary range
- $130,000–$310,000
Listed salaries for Fate Therapeutics Inc. roles on Migrate Mate range from about $130,000 to $310,000 per year across 6 open roles, as of July 15, 2026.
Open Roles at Fate Therapeutics Inc.
Showing 6 of 6+ Fate Therapeutics Inc. jobs
Fate Therapeutics is seeking a scientifically rigorous and highly motivated Clinical Scientist to join our Clinical Development team. The Clinical Scientist will play a key role in advancing our pipeline of highly innovative cell therapies from early clinical development through regulatory approval. As a key scientific partner to the clinical study team, the Clinical Scientist will support the design, execution, and interpretation of clinical studies while ensuring the highest standards of ethical conduct, patient safety, and adherence to GCP compliance. This key member of the clinical team will collaborate closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Medical Writing, and Biometrics, to advance clinical programs. This is a full-time, exempt position located at our corporate headquarters in San Diego, CA.
Responsibilities
- Collaborate in the review, analysis, and interpretation of emerging study data from clinical trials across the program, ensuring data integrity and study conduct is performed with the highest level of ethical and safety standards and in compliance with all regulatory requirements.
- Partner with the study team to develop key strategic documents, including eCRFs, clinical study plans, protocols and reports.
- Contribute to the review and presentation of clinical sections of regulatory documents including Investigators’ Brochures, briefing books, safety updates, IND/NDA submission documents, study protocols, informed consents, statistical analysis plans, regulatory approval submissions, serious and non-serious adverse event evaluation, and responses to Health Authorities inquiries.
- Stay current on standards of practice within relevant therapeutic areas to support strategic discussion and decision-making for the program.
- Support data review activities including ongoing data cleaning through database lock, ensuring safety and response data reconciliation, review of medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends, and review of data tables, listings, and figures; and clinical study reports.
- Develop effective working relationships with key investigators and coordinators to optimize scientific quality and innovation of clinical study design, execution, reporting and publications.
- Support the contributions to meetings for trial-related advisory boards, investigators, safety monitoring, and study team training.
- Coordinate with internal and external study teams the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic and biomarker data, to provide consolidated information for Senior Management.
- Assist in forecasting trial resource needs (internal and external).
Qualifications
- MS, RN, PhD, or PharmD with a minimum of 3 years technical and/or operational experience in planning, executing, reporting, and publishing clinical studies in a biotech, pharmaceutical, or CRO environment.
- Experience in the design and conduct of oncology or autoimmune clinical trials is desirable.
- Experience in novel combinations and innovative designs for early phase studies.
- Proven experience writing and presenting scientific communications with clarity, accuracy, and rigor.
- Experience with U.S. and European regulatory authorities and submissions is desirable.
- Experience or exposure to the development of cell therapies is desirable.
- Self-motivation, good judgment, strong follow up, organizational, analytical, and problem-solving skills; capable of identifying risks; creative and innovative thinker.
- Ability to work with, lead, and motivate a cross-functional matrix team.
- Excellent written and oral communication skills. Ability to communicate effectively with cross-functional teams and through formal presentation and scientific discussion ensuring credibility, accuracy, and confidence with internal and external stakeholders and experts.
Working conditions & physical requirements
- Travel may be required (up to 10%).
- Subject to extended periods of sitting and standing, vision to monitors, and moderate noise levels.
Compensation
- The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location.
- Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package.
- The anticipated salary range for this role is $130,000 - $150,000.
Equal Employment Opportunity
Privacy Notice
About Fate Therapeutics, Inc.
️ Recruitment Fraud Alert
- Our Talent Acquisition team only corresponds from our @fatetherapeutics.com domain.
- At no stage in our hiring process will we require payment or ask you to make deposits in your bank account.
- We will only ask for personal information when applying for a position via our Careers page or thereafter.
- At no stage during our hiring process will we ask you to click a link to begin a one-way video interview.
- We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. 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.
Fate Therapeutics is seeking a scientifically rigorous and highly motivated Clinical Scientist to join our Clinical Development team. The Clinical Scientist will play a key role in advancing our pipeline of highly innovative cell therapies from early clinical development through regulatory approval. As a key scientific partner to the clinical study team, the Clinical Scientist will support the design, execution, and interpretation of clinical studies while ensuring the highest standards of ethical conduct, patient safety, and adherence to GCP compliance. This key member of the clinical team will collaborate closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Medical Writing, and Biometrics, to advance clinical programs. This is a full-time, exempt position located at our corporate headquarters in San Diego, CA.
Responsibilities
- Collaborate in the review, analysis, and interpretation of emerging study data from clinical trials across the program, ensuring data integrity and study conduct is performed with the highest level of ethical and safety standards and in compliance with all regulatory requirements.
- Partner with the study team to develop key strategic documents, including eCRFs, clinical study plans, protocols and reports.
- Contribute to the review and presentation of clinical sections of regulatory documents including Investigators’ Brochures, briefing books, safety updates, IND/NDA submission documents, study protocols, informed consents, statistical analysis plans, regulatory approval submissions, serious and non-serious adverse event evaluation, and responses to Health Authorities inquiries.
- Stay current on standards of practice within relevant therapeutic areas to support strategic discussion and decision-making for the program.
- Support data review activities including ongoing data cleaning through database lock, ensuring safety and response data reconciliation, review of medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends, and review of data tables, listings, and figures; and clinical study reports.
- Develop effective working relationships with key investigators and coordinators to optimize scientific quality and innovation of clinical study design, execution, reporting and publications.
- Support the contributions to meetings for trial-related advisory boards, investigators, safety monitoring, and study team training.
- Coordinate with internal and external study teams the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic and biomarker data, to provide consolidated information for Senior Management.
- Assist in forecasting trial resource needs (internal and external).
Qualifications
- MS, RN, PhD, or PharmD with a minimum of 3 years technical and/or operational experience in planning, executing, reporting, and publishing clinical studies in a biotech, pharmaceutical, or CRO environment.
- Experience in the design and conduct of oncology or autoimmune clinical trials is desirable.
- Experience in novel combinations and innovative designs for early phase studies.
- Proven experience writing and presenting scientific communications with clarity, accuracy, and rigor.
- Experience with U.S. and European regulatory authorities and submissions is desirable.
- Experience or exposure to the development of cell therapies is desirable.
- Self-motivation, good judgment, strong follow up, organizational, analytical, and problem-solving skills; capable of identifying risks; creative and innovative thinker.
- Ability to work with, lead, and motivate a cross-functional matrix team.
- Excellent written and oral communication skills. Ability to communicate effectively with cross-functional teams and through formal presentation and scientific discussion ensuring credibility, accuracy, and confidence with internal and external stakeholders and experts.
Working conditions & physical requirements
- Travel may be required (up to 10%).
- Subject to extended periods of sitting and standing, vision to monitors, and moderate noise levels.
Compensation
- The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location.
- Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package.
- The anticipated salary range for this role is $130,000 - $150,000.
Equal Employment Opportunity
Privacy Notice
About Fate Therapeutics, Inc.
️ Recruitment Fraud Alert
- Our Talent Acquisition team only corresponds from our @fatetherapeutics.com domain.
- At no stage in our hiring process will we require payment or ask you to make deposits in your bank account.
- We will only ask for personal information when applying for a position via our Careers page or thereafter.
- At no stage during our hiring process will we ask you to click a link to begin a one-way video interview.
- We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. 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.
Job Roles at Fate Therapeutics Inc.
Working at Fate Therapeutics Inc.
Fate Therapeutics Inc.'s 6 open roles are manager level or above, and about 0% are remote or hybrid. The most active teams are nursing, procurement & supply chain, and clinical trials & medical research. Fate Therapeutics is a clinical-stage biopharmaceutical company that develops cellular immunotherapy products, with open positions spanning medical affairs, regulatory affairs, clinical science, and supply chain. Most Fate Therapeutics Inc. roles are based in San Diego.
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Browse jobs by roleFate Therapeutics Inc. Jobs: Frequently Asked Questions
How many jobs is Fate Therapeutics Inc. hiring for right now?
Fate Therapeutics Inc. is hiring for 6 open roles on Migrate Mate as of July 15, 2026, updated daily, concentrated in nursing and procurement & supply chain. Roles span medical affairs, regulatory affairs, clinical science, and supply chain functions across the organization.
What kinds of roles does Fate Therapeutics Inc. hire for?
The most active teams are nursing, procurement & supply chain, and clinical trials & medical research. Fate Therapeutics hires across clinical, regulatory, medical, and supply chain functions, with positions such as Medical Director, Clinical Scientist, Director of Regulatory Affairs, and Senior Director of Supply Chain. Most postings are manager level or above, reflecting the specialized expertise required in biopharmaceutical drug development.
Are Fate Therapeutics Inc. jobs remote or in-person?
Mostly on-site. About 0% of Fate Therapeutics Inc.'s open roles on Migrate Mate are remote or hybrid as of July 15, 2026, with the rest based in San Diego. Each Fate Therapeutics Inc. listing shows its work location so you can filter before applying.
How do I apply to a job at Fate Therapeutics Inc.?
Find a role that matches your background among Fate Therapeutics Inc.'s open listings on Migrate Mate, then follow the link through to Fate Therapeutics' own careers page to submit your application directly. Fate Therapeutics manages its own hiring process, so all applications, status updates, and interview coordination are handled by their team.
What do Fate Therapeutics Inc. jobs pay?
Listed salaries for Fate Therapeutics Inc. roles on Migrate Mate range from about $130,000 to $310,000 per year as of July 15, 2026, with most postings at manager level or above. Exact pay is set by Fate Therapeutics Inc. and shown on each listing.
Does Fate Therapeutics Inc. hire entry-level?
Most of Fate Therapeutics Inc.'s open roles on Migrate Mate are manager level or above as of July 15, 2026. Entry-level openings are limited. Check individual Fate Therapeutics Inc. listings for stated experience requirements.
Where is Fate Therapeutics Inc. hiring?
Most Fate Therapeutics Inc. roles are based in San Diego, and about 0% offer remote or hybrid work as of July 15, 2026. Migrate Mate shows the location on each listing.