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Director Cell Therapy Research Development Jobs

... research experiments and analytical studies to identify and validate potential novel drug targets ... therapies; * Background in drug discovery and development in the pharmaceutical industry;

... research experiments and analytical studies to identify and validate potential novel drug targets ... therapies; * Background in drug discovery and development in the pharmaceutical industry;

... and cell therapy manufacturing. Our mission is deeply meaningful, and we're looking for bold ... direct your inquiries to our HR Department (fcdi-hr@fujifilm.com). Salary: . Date posted: 02/23 ...

... cell therapies. The Marketplace Director operates with an ownership mindset, leads through ... Own regional business results by leading the development, execution, and monitoring of integrated ...

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Director Cell Therapy Research Development information

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$65.5K

$162.7K

$215K

How much do director cell therapy research development jobs pay per year?

As of Sep 9, 2026, the average yearly pay for director cell therapy research development in the United States is $162,707.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,000.00 and $194,000.00 per year, depending on experience, location, and employer.

What does a director of cell therapy research development do?

A Director of Cell Therapy Research Development leads and manages research initiatives focused on developing new cell-based therapies, such as those used in cancer treatment or regenerative medicine. They oversee scientific teams, design research strategies, manage budgets, and ensure compliance with regulatory standards. This role also involves collaborating with clinical teams, regulatory agencies, and industry partners to advance therapies from the laboratory to clinical trials and ultimately to patients. Their leadership is crucial for driving innovation and ensuring that research projects meet both scientific and business objectives.

What are the key skills and qualifications needed to thrive as a director of cell therapy research development?

To thrive as a Director of Cell Therapy Research Development, you need advanced expertise in cellular biology, immunology, and drug development, typically supported by a PhD or MD and extensive experience in cell therapy research. Familiarity with regulatory requirements, Good Manufacturing Practice (GMP) standards, and laboratory management systems is crucial. Strong leadership, strategic vision, and the ability to communicate complex concepts clearly help drive innovation and collaboration across multidisciplinary teams. These skills ensure the successful development and translation of cell therapy products from research to clinical application, meeting both scientific and regulatory milestones.

What are some common challenges faced by a director of cell therapy research development, and how can they be addressed?

A Director of Cell Therapy Research Development often faces challenges such as managing cross-functional teams, navigating regulatory complexities, and ensuring the scalability of new therapies from research to clinical application. Addressing these challenges requires strong leadership, effective communication, and close collaboration with regulatory, clinical, and manufacturing partners. Staying current with industry trends and fostering a culture of innovation and compliance can also help overcome obstacles and drive successful project outcomes.

What is the difference between Director Cell Therapy Research Development vs Cell Therapy Research Scientist?

AspectDirector Cell Therapy Research DevelopmentCell Therapy Research Scientist
CredentialsAdvanced degrees (PhD, MD), extensive experience in cell therapyTypically a PhD or Master's in related fields
Work EnvironmentLeadership roles in R&D departments, strategic planningLaboratory research, experimental design, data analysis
Employer & Industry UsageBiotech and pharmaceutical companies, clinical research organizationsResearch institutions, biotech firms, academic labs
Search & Comparison IntentUnderstanding leadership roles, career progressionResearch activities, technical skills

The main difference between a Director Cell Therapy Research Development and a Cell Therapy Research Scientist lies in their responsibilities and experience level. The director oversees strategic planning, manages teams, and guides development projects, while the scientist focuses on conducting experiments and generating data. Both roles require strong expertise in cell therapy, but the director typically has more leadership and managerial duties.

What are popular job titles related to Director Cell Therapy Research Development jobs?

For Director Cell Therapy Research Development jobs, the most frequently searched job titles are:

Infographic showing various Director Cell Therapy Research Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $162,707 per year, or $78.2 per hour.

Associate Director, Cell Therapy Operations- Southeast

Jacksonville, FL • Remote

Novartis
Pharmaceutical and Medicine Manufacturing • 10K+ employees

$138K - $257K/yr

Full-time

Medical, Retirement, PTO

Re-posted 17 days ago


Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

Job Description Summary

#LI-Remote
The Associate Director Cell Therapy Operations Manager is in the Southeast geography. This is a remote& field-based role that covers thefollowing, butnot limited to:Atlanta, GA, Charlotte, NC and Jacksonville, FL. Associatemustresidewithin territory, or within a reasonable daily commuting distance of 60 miles from territory.
The Associate Director, Cell Therapy Operations Manager (AD, CTOM) is a field-based operational leader responsible for training, onboarding, and qualifying CAR-T treatment centers to support the safe, compliant, and successful delivery of Novartis CAR-T therapies. The AD, CTOM serves as the primary operational partner to assigned treatment centers, supporting ordering, logistics, apheresis collection, site readiness, quality compliance, and operational excellence while collaborating cross-functionally to resolve complex challenges and improve site performance.


Job Description

Major Accountabilities
  • Execute onboarding, training, qualification, and operational readiness activities for CAR-T treatment centers to support successful site activation and patient treatment.
  • Serve as the field-based operational lead for assigned treatment centers, supporting ordering, logistics, apheresis collection, product receipt, and treatment workflows.
  • Deliver high-quality operational support to treatment centers, care teams, and internal stakeholders to ensure consistent execution of CAR-T processes.
  • Resolve complex operational challenges related to ordering, logistics, apheresis collection, product handling, and site readiness.
  • Ensure compliance with operational, regulatory, quality, and procedural requirements, supporting ongoing inspection and audit readiness.
  • Lead site readiness, operational continuity, and refresher training initiatives to maintain consistent performance and adherence to Novartis standards.
  • Partner cross-functionally with Patient Support, Strategic Account Managers, Quality, Manufacturing, Clinical Operations, Medical Affairs, and other stakeholders to align strategy, improve processes, and drive successful patient outcomes.
  • Identify operational risks, implement process improvements, manage escalations, and drive continuous improvement initiatives across assigned treatment centers.
Minimum Requirements

Education: Bachelor's degree in science, healthcare, nursing, business, or a related discipline.

  • Minimum 7 years of healthcare, pharmaceutical, biotechnology, specialty operations, or related industry experience.
  • Experience supporting complex healthcare systems, treatment centers, academic medical centers, or multi-site institutions.
  • Demonstrated experience in cell therapy operations, specialty therapy operations, or other highly regulated healthcare environments.
  • Proven experience training, onboarding, educating, or supporting external healthcare stakeholders.
  • Ability to effectively operate within matrixed, cross-functional organizations and influence stakeholders without direct authority.
  • Strong project management, problem-solving, and operational execution skills with the ability to manage multiple priorities simultaneously.
  • Excellent communication, presentation, and relationship-management skills with internal and external stakeholders.

Candidate must reside within territory, or within a reasonable daily commuting distance of 60 miles from the territory border. Ability to travel 60-80% over a broad geography is required, with the ability to drive and/or fly within the territory. Must have a valid driver's license.

Preferred Qualifications
  • Direct experience supporting CAR-T, cell therapy, apheresis, blood or tissue collection, cryopreservation, transplant, or related specialty operations.
  • Experience working within GxP-regulated pharmaceutical, biotechnology, manufacturing, cell processing, hospital, or specialty healthcare environments.

The pay range for this position at commencement of employment is expected to be between$138,600.00 and $257,400.00/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$138,600.00 - $257,400.00


Skills Desired

Adaptive Strategy And Innovation (Inactive), Clinical Research, Cross-Functional Teamwork, Drug Development, Financial Management, Interpersonal Communication Skills (Inactive), Microsoft Project, Pmi (Project Management Institute) (Inactive), Pmp (Project Management Professional) (Inactive), Product Development, Program Management, Project Delivery, Project Implementations, Project Management Life Cycle (PMLC), Project Planning, R&D (Research And Development) (Inactive), Resource Allocation, Risk Management, Senior Management (Inactive), Stakeholder Management, Time Management Skills (Inactive), Waterfall Model

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