Associate Director, Cell Therapy Territory Operations Manager
Cleveland, TN - USA
Job Summary
In AstraZenecas Cell Therapy division we follow the science to explore and innovate. We are working towards treating preventing modifying and even curing some of the worlds most complex diseases. We have the potential to grow our pipeline and positively impact the lives of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.
The Associate Director Territory Operations Manager (AD-TOM) is a regional expert supporting Patient Operations and project teams in cell therapy. As a senior technical leader the role sets and implements compliant policies and standards for treatment centers partners with Regional Operations Directors (RODs) on site strategy leads research and internal reporting and maintains up-to-date best practices.
The role expands AZs cell therapy footprint in oncology by building patient-centered service lines and leading complex engagements with site leadership and frontline providers. It delivers operational and clinical guidance for trials and commercial products leads site activation and provides ongoing operational quality and clinical oversight AD-TOM is a field regional role supporting the Midwestern territory (with preference for candidate to be based in Ohio or Michigan) and will report to a Regional Operations Director (ROD).
You Will:
Lead and support strategic initiatives across clinical and commercial cell therapy from development to post-market.
Be a key leader within Internal AZ teams (Program Management QA Manufacturing Supply Chain Medical Affairs Market Access Compliance Sales/Marketing).
Establish service lines with external partners (PIs Physicians Nursing Apheresis Cell Therapy Lab other HCPs/leadership).
Serve as SME driving decisions and projects at multi-country/local levels; influence strategy governance and cross-functional execution.
Acts as the technical expert and authoritative source of knowledge in cell therapy workflows and brings expertise to site interactions.
Build and maintain relationships with stakeholders at assigned Sites.
Operate within regulatory/accreditation standards (e.g. FACT) ensuring compliance audit readiness and continuous improvement.
Guide clinical workflows; ensure standards; advance apheresis excellence; optimize product handling; inform health outcomes.
Act as primary operations readiness liaison; collaborate with Supply Chain to align logistics and site needs.
Provide exemplary customer service while building business relations with clinical/operational leaders.
Lead cross-functional meetings to develop product/patient workflows for trials and future commercial products.
Maintain strong collaboration with Program Management SMM Supply Chain Manufacturing Quality Medical Commercial Cell Therapy Hub to manage customer centers and clinical care for the portfolio.
Oversee operational/clinical aspects of raw material collection product receipt/storage/distribution/infusion and COI/COC.
Design and deliver training to PIs MD Nursing Staff Apheresis and Cell Therapy Laboratory and Coordinator staff
Lead Site activation using risk-based tools for certification training and monitoring.
Train Site HCPs on product needs; ensure COI/COC access for trained individuals with Cell Therapy Hub.
Oversee Site logistics and manage regional account changes with Cell Therapy Hub.
Respond to SOP deviations with expertise and collegiality.
Support/own quality records (Deviations CAPA Change Control) with Cell Therapy Hub and QA.
Travel up to 50%.
You Have:
Bachelors degree (Nursing Physician Assistant) with thorough knowledge/hands-on experience in Cell Therapy.
8 years experience in cell therapy with progressive leadership.
Expertise in service lines (infrastructure resourcing costs quality metrics).
Proven delivery to timelines cost and quality; collaboration with internal/external providers.
Excellent knowledge of cell therapy standards/regulations.
Experience selecting/overseeing external providers and developing contracts.
Nice to Have:
Advanced scientific degree; broad understanding across patient operations manufacturing interfaces quality regulatory market access; project management experience.
Program/Quality qualifications (e.g. PMP CPHQ).
Experience across academic/Sponsor settings and countries.
Early-phase delivery across product lifecycle and multiple therapeutic areas.
Salesforce or similar CRM experience.
#celltherapy
The annual base pay for this position ranges from $150K to $225K. Our positions offer eligibility for various incentivesan 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
07-Apr-2026Closing Date
30-Apr-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and furtherance of that mission we welcome and consider applications from all qualified candidates regardless of their protected characteristics. If you have a disability or special need that requires accommodation please complete the corresponding section in the application form.
Required Experience:
Director
About Company
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more