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Associate Director, Cell Therapy Territory Operations Manager

8+ years
$150,000 – $225,000
10 Nov. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director – Cell Therapy Territory Operations Manager

Location: Wilmington, Delaware, United States
Job ID: R-237631
Posted On: 12-Nov-2025
Closing Date: 25-Nov-2025


About the Role

The Associate Director – Territory Operations Manager (AD-TOM) plays a senior regional role within AstraZeneca’s Cell Therapy division. This position supports Patient Operations, site activation, clinical workflows, and ongoing operational excellence across the Northern Atlantic territory. The role combines scientific, operational, and strategic responsibilities to expand AZ’s cell therapy footprint in oncology.

This is a field-based regional position with preference for candidates located in:
New York, Massachusetts, Pennsylvania, New Jersey, Rhode Island, or Connecticut.

You will report directly to the Regional Operations Director (ROD).


Key Responsibilities

Strategic & Cross-Functional Leadership

  • Lead and support strategic initiatives across clinical and commercial cell therapy—from development to post-market.

  • Serve as a key leader across internal AZ teams: Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/Marketing.

  • Act as SME (Subject Matter Expert) influencing multi-country or regional strategies, governance, and execution.

External Collaboration & Service Line Development

  • Establish and manage service lines with external partners such as PIs, physicians, nurses, apheresis teams, and cell therapy labs.

  • Build and maintain strong relationships with leadership and HCPs at assigned Sites.

  • Deliver exemplary customer service and support clinical/operational leaders.

Clinical & Operational Oversight

  • Provide operational and clinical guidance for trials and commercial cell therapy products.

  • Lead site activation using risk-based processes for certification, training, and monitoring.

  • Guide apheresis excellence, product handling optimization, and clinical workflow standards.

  • Oversee raw material collection, product receipt/storage/distribution/infusion, and COI/COC processes.

Quality & Compliance

  • Ensure regulatory/accreditation compliance (e.g., FACT).

  • Maintain audit readiness and drive continuous improvement.

  • Support or own quality records (Deviations, CAPA, Change Control) with Cell Therapy Hub and QA.

Training & Education

  • Design and deliver training for PIs, MDs, nursing, apheresis teams, and cell therapy laboratory staff.

  • Train site HCPs on product requirements and ensure COI/COC access.

Logistics & Coordination

  • Act as primary operations readiness liaison.

  • Work with Supply Chain to align logistics with site needs.

  • Oversee site logistics and manage changes via the Cell Therapy Hub.

Cross-Functional Project Execution

  • Lead meetings to develop product/patient workflows for trials and commercial programs.

  • Collaborate with Program Management, Manufacturing, Quality, Supply Chain, and Medical teams.

Travel

  • Travel requirement up to 50%.


Required Qualifications

  • Bachelor’s degree (e.g., Nursing, Physician Assistant) with deep knowledge and hands-on cell therapy experience.

  • 8+ years of progressive experience in cell therapy.

  • Expertise in service line development: infrastructure, resource planning, cost, quality metrics.

  • Proven record of meeting timeline, cost, and quality goals.

  • Strong knowledge of cell therapy standards and regulations.

  • Experience selecting and managing external providers and contracts.


Preferred Qualifications

  • Advanced scientific degree.

  • Broad understanding of patient operations, manufacturing, quality, regulatory, and market access.

  • Project management certifications (e.g., PMP, CPHQ).

  • Experience across academic and Sponsor settings, including cross-country exposure.

  • Early-phase product lifecycle experience across multiple therapeutic areas.

  • Salesforce or CRM experience.


Compensation & Benefits

  • Annual Base Pay: $150,000 – $225,000

  • Eligibility for:

    • Short-term incentive bonuses

    • Equity-based awards

    • Commissions (applicable for sales roles)

  • Benefits include:

    • Retirement programs

    • Paid time off (vacation, holiday, leaves)

    • Health, dental, and vision insurance (as per applicable plans)


Equal Opportunity Statement

AstraZeneca is committed to creating an inclusive workplace. All qualified applicants will receive equal consideration regardless of protected characteristics. Applicants with disabilities or special needs may request reasonable accommodations through the application form.