Senior Manager / Manager, Regulatory Affairs (Clinical)
- Employer
- Fate Therapeutics
- Location
- San Diego, CA, United States
- Start date
- Jun 20, 2021
View more
- Discipline
- Clinical, Clinical Research, Regulatory, Regulatory Affairs
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Biotech Beach
Job Details
Responsibilities
• Effectively work with internal and external stakeholders to independently manage clinical regulatory activities under the direction of the RA Clinical Lead
• Manage, author, coordinate, and review regulatory submission documents and development activities to support regulatory filings and dossier lifecycle
• Work with the clinical team to provide regulatory review of clinical study protocols, ICFs, SAPs, and CSRs
• Independently research and interpret regulations, and provide regulatory guidance to cross-functional stakeholders; monitor clinical industry and regulatory trends and be able to apply learnings and provide guidance related to such trends
• Establish functional processes, guidelines, and SOP's
• Support the strategy and preparation of health authority meeting materials and responses to requests for information under the direction of the RA Clinical Lead
• Support management with development and implementation of departmental strategies and policies, and contribute to the development and implementation of regulatory strategies to mitigate risks
• Assure compliance with all applicable (domestic and international) regulations
• May mentor or provide oversight of assigned department staff
• Other duties as assigned
Requirements
• A minimum of a Bachelors' degree in a life science with at least 5 years of experience in RA in
the biotechnology or pharmaceutical industries
• Demonstrated direct experience with Health Authority submissions and strong knowledge of FDA/EMA regulations and agency submission and approval processes
• Proven experience in applying regulatory knowledge to various clinical activities; strong knowledge of clinical study design, Good Clinical Practice principles, and navigation of clinical development pathways
• Experience leading and managing the preparation of annual reports, DSURs, and Investigator's Brochures
• Strong ability to quickly absorb new technical and strategic information and have the flexibility to adapt accordingly
• Excellent operational skills including planning, organizing, and the ability to deal effectively with a variety of personnel both internally and outside the company to drive projects to timely completion
• Excellent writing, communication, and interpretive skills
• High attention to detail, ability to work on multiple projects with tight deadlines and able to work independently
• Previous cell therapy product experience and regulatory knowledge is highly preferred
• Prior direct interactions with Health Authorities is desirable
• Prior participation in a GCP inspection is desirable
• Experience with CTA filing preferred
Working Conditions and Physical Requirements
• May require occasional evening and weekend work
• Full-time onsite work at Company's headquarters in San Diego
• May require occasional travel for training programs and meetings
The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time.
For consideration send cover letter and resume to: careers@fatetherapeutics.com and reference job 480VM.
About Fate Therapeutics, Inc.
Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer. The Company has established a leadership position in the clinical development and manufacture of universal, off-the-shelf cell products using its proprietary induced pluripotent stem cell (iPSC) product platform. The Company's immuno-oncology pipeline includes off-the-shelf, iPSC-derived natural killer (NK) cell and T-cell product candidates, which are designed to synergize with well-established cancer therapies, including immune checkpoint inhibitors and monoclonal antibodies, and to target tumor-associated antigens using chimeric antigen receptors (CARs). The Company's pipeline also includes ProTmune™, a pharmacologically modulated, donor cell graft that is currently being evaluated in a Phase 2 clinical trial for the prevention of graft-versus-host disease in patients with hematologic malignancies undergoing allogeneic stem cell transplant. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit www.fatetherapeutics.com.
Company
Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a first-in-class pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients with cancer and autoimmune disorders. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company’s effector cell pipeline includes multiplexed-engineered, iPSC-derived natural killer (NK) cell and T-cell product candidates, which incorporate novel synthetic controls of cell function, such as chimeric antigen receptors (CARs) to target tumor-associated antigens and are intended to deliver multiple mechanisms of therapeutic importance to patients including in combination with well-established cancer therapies. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit www.fatetherapeutics.com.
- Website
- http://www.fatetherapeutics.com/
- Phone
- 858.875.1800
- Location
-
12278 Scripps Summit Drive
San Diego
California
92131
United States
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