AstraZeneca

Executive Director, Head of Cell Therapy Non-Clinical Safety Lead, Cell Therapy Translational and Safety Sciences.

AstraZeneca$264K — $396K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Toxicology, Biology, or Immunology with over 10 years of experience.
  • Deep expertise in nonclinical safety relating to CAR-T and TCR cell therapies.
  • History of supporting nonclinical safety evaluations of diverse cell therapy modalities.
  • Experience with global regulatory submissions (IND/BLA/IIT) and regulatory interactions.
  • Strong leadership with proven talent development and team management skills.
  • Background in enhancing pre-clinical safety for T-cell therapies through collaborations.

Responsibilities

  • Lead a global team focused on safe cell therapy design across various platforms.
  • Ensure resource allocation and project prioritization for a dynamic cell therapy portfolio.
  • Develop talent within the team and promote inclusion and diversity.
  • Influence project strategies using expertise in Nonclinical Cell Therapy Safety.
  • Accountable for overall strategy and deliverables in Cell Therapy Safety Sciences.
  • Foster collaborations and networks with key global stakeholders.
  • Evaluate business development opportunities related to cell therapies.

Benefits

  • Retirement program participation.
  • Paid time off including vacation, holidays, and leaves.
  • Health, dental, and vision insurance coverage.
Full Job Description

 Are you passionate about shaping the future of Cell Therapy? We are seeking an entrepreneurial leader to head our Nonclinical Safety Sciences team in our new global multi-functional Cell Therapy Translational and Safety Sciences group.  As the Nonclinical Safety Sciences Head, you will play a crucial role in bringing the next generation of innovative life-changing medicines to patients. You will oversee a team of toxicologists and laboratory-based specialists to influence and enable the design and development of safe cell therapies across multiple modalities and therapeutic areas.   You will report to the VP of Cell Therapy Translational and Safety Sciences (CT-TSS) and will become a member of the CT-TSS Leadership Team contributing to both, strategy and operational discussions and initiatives.   


Key Responsibilities: 


•    Lead global team of toxicologists and laboratory-based specialists to design and deliver safe cell therapies, across different platforms (autologous, allogeneic, in vivo), engineered with CAR-T and TCR-T, and across therapeutic areas.
•    Ensure appropriate resource allocation and program and project prioritization for timely delivery towards a dynamic and expanding cell therapy portfolio. Provide oversight and guidance to enable project and portfolio investment decisions.
•    Lead and manage talent development, recruitment and evaluate team performance on a regular basis. Promote inclusion and diversity to build high-functioning teams within and across departments. Align to AZ’s culture and values and further solidify our reputation as a great place to work.  
•    As a seasoned subject matter expert in Nonclinical Cell Therapy Safety, use experience, expertise and leadership to influence Cell Therapy Safety Science project strategies. Anticipate and manage potential project-related nonclinical safety concerns and support global regulatory submissions and health authority requests.   
•    Be responsible and accountable for Cell Therapy Safety Sciences strategy and deliverables.
•    Build and promote collaborative and inclusive networks and workstreams to ensure alignment with key global stakeholders.   
•    Initiate, lead and manage internal and external collaborations to access latest scientific developments and innovations, expanding business opportunities for the company resulting in enhanced impact and external scientific leadership in the field of cell therapy.  
•    Performs business development-related asset, platform or technology evaluations .
•    Perform evaluation and due diligence for in licensing, out-sourcing or collaboration opportunities.  
•    Contribute to wider scientific strategy on cell therapy within the Cell Therapy Enterprise and cross-functionally with relevant partners in AZ.  

Requirements:  


•    PhD relevant field (Toxicology, Biology, Immunology) with over 10 years of experience.
•    Excellent understanding of nonclinical safety sciences in the context of CAR-T & TCR cell therapies and proven prior experience in the field.  
•    Extensive experience supporting nonclinical safety assessments of cell therapies, including different modalities and platforms (autologous, allogeneic, in vivo, etc), from target identification through clinical development.   
•    Experience of global IND / BLA / IIT submissions, leading regulatory interactions within area of expertise and responding to global regulatory questions.   
•    Proven and excellent experience in designing, developing and implementing cell therapy safety strategies.  
•    Strong leadership skills and line management experience with a positive team engaging attitude and a track record in the leadership, management and talent development of individuals and teams.  
•    Track record of leading impact on drug R&D within the pharmaceutical industry or biotech sector with a strong focus on safety assessment.
•    Leader of collaborations with academia, biotech and / or pharma industry to enhance pre-clinical safety assessment of T-cell therapies.
•    Track record of scientific innovation in the safety assessment arena  
•    Recognized as a leader and influencer in the cell therapy field with proven track record of publishing relevant results and tools in journals, conferences, and other scientific proceedings.  

In Office Requirement:  
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. 
  
Interested? Come join our journey.    

 The annual base pay for this position ranges from $264,258.40 - $396,387.60 Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

04-Aug-2026

Closing Date

30-Aug-2026

About AstraZeneca

AstraZeneca is a British-Swedish multinational pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs. The company was formed in 1999 through the merger of Astra AB and Zeneca Group plc. AstraZeneca's products are used to treat a wide range of medical conditions, including cancer, cardiovascular disease, respiratory disease, and diabetes. The company has operations in over 100 countries and employs more than 76,000 people worldwide. AstraZeneca is committed to developing innovative medicines that improve the health and well-being of people around the world.
Learn more about AstraZeneca
Size
83,100 employees
Market Cap
$211.5 billion
Industry
Net Income
$3.1 billion
Founded
1999
5 Year Trend
+10.2%
Revenue
$26.6 billion
NASDAQ

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