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Cell Therapy Project Manager Jobs (NOW HIRING)

$66K - $99K/yr

Production Specialist II Cell Therapy Cell Culture - Berkeley, CA As a Prod Spec II Cell Therapy ... Experience with Lean manufacturing methods and continuous improvement projects.Employees can expect ...

Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy ... Legend Biotech is seeking a Manager, Regulatory Project Management as part of the Regulatory team ...

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Cell Therapy Project Manager information

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$38.5K

$102.7K

$162K

How much do cell therapy project manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for cell therapy project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What does a cell therapy project manager do?

A Cell Therapy Project Manager oversees the planning, execution, and completion of projects related to cell therapy development and manufacturing. They coordinate cross-functional teams, manage timelines and budgets, and ensure regulatory and quality compliance throughout the project lifecycle. Their role is critical in bridging scientific, operational, and business aspects to successfully deliver advanced cell therapy products.

What are the key skills and qualifications needed to thrive as a cell therapy project manager?

To thrive as a Cell Therapy Project Manager, you need expertise in project management, a strong background in life sciences or biomedical fields, and experience in cell therapy or related biopharmaceutical areas. Familiarity with project management software (e.g., MS Project), regulatory systems like FDA/EMA guidelines, and certifications such as PMP are highly valuable. Outstanding communication, problem-solving, and leadership skills help drive multidisciplinary teams and manage complex timelines. These competencies ensure successful coordination, regulatory compliance, and timely delivery of cutting-edge cell therapy projects.

What are some common challenges faced by cell therapy project managers when coordinating cross-functional teams?

Cell Therapy Project Managers often navigate the complexities of coordinating among scientists, regulatory specialists, manufacturing teams, and clinical operations. A common challenge is aligning timelines and expectations across these diverse groups, especially since cell therapy projects are highly regulated and subject to evolving guidelines. Effective communication, proactive issue resolution, and adaptability are crucial for overcoming these obstacles and ensuring project milestones are met. Building strong relationships with stakeholders and maintaining clear documentation also help mitigate risks and keep projects on track.

What is the difference between Cell Therapy Project Manager vs Clinical Research Associate?

AspectCell Therapy Project ManagerClinical Research Associate
Required CredentialsBachelor's degree in life sciences, project management experience, industry certificationsBachelor's degree in life sciences, clinical research experience, regulatory knowledge
Work EnvironmentBiotech or pharmaceutical companies, overseeing cell therapy projectsClinical trial sites, monitoring clinical study progress
Employer & Industry UsageUsed in biotech firms developing cell therapiesCommon in clinical research organizations and pharma companies
Search & Comparison IntentUnderstanding project management roles in cell therapyComparing clinical trial monitoring roles

The Cell Therapy Project Manager focuses on overseeing cell therapy development projects, coordinating teams, and managing timelines. In contrast, a Clinical Research Associate primarily monitors clinical trials at study sites, ensuring compliance and data integrity. While both roles require scientific backgrounds and industry experience, their responsibilities differ in scope and focus within the clinical development process.

What are popular job titles related to Cell Therapy Project Manager jobs?

For Cell Therapy Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Cell Therapy Project Manager job openings in the United States as of September 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Senior Director, Global Project Management, Cell Therapy

Gaithersburg, MD • Hybrid

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz


Job description

Senior Director, Global Project Management, Cell Therapy Gaithersburg, MD, candidates from Boston, MA will also be considered Global Portfolio & Project Management (GPPM) Hybrid Work- on average 3 days/week in office The Senior Director, Global Project Management, Cell Therapy is a key leadership position, accountable for the project management of Global Project Teams (GPTs), working alongside Global Product, Scientific, Clinical Commercial Leaders to establish the brand strategy and deliver the approved project plans. You will be assigned to lead programmes of the highest complexity and priority and are regarded as key leaders within the GPT and GPPM organization. This is a critical and exciting opportunity to use your scientific knowledge and strategic expertise to lead and influence decisions that will have a direct impact on patients' lives.

Working at the highest levels, you will ensure the decisions we make position AstraZeneca for maximum return on investment and positive patient outcomes. What you'll do Strategic Business Partnership Provide program management leadership and excellence through active input into the project strategy ensuring alignment of the program strategy with operational reality Lead development of drug project, cross-project, or portfolio strategies Where applicable, work with alliance partners and run joint alliance forums and governance committee Identify key business opportunities or needs for strategic shifts based on external and internal events Partner with Business Development to provide strategic input to potential deal cases (investment & divestment) Ensure appropriate linkages between project strategy and key internal processes (TA strategy, TA prioritization, corporate scorecard) Cross-functional Team Leadership and Delivery Lead project management of cross functional drug development teams and ensure delivery of strategic objectives Create a shared sense of purpose, inspiring and energising others to build and maintain a cohesive High Performing Team. Coach project teams and GPT towards successful issue resolution and decision making.

Engage with critical stakeholders to address barriers or challenges facing team Focus the GPT on the right activities at the right time. Coordinate the efforts of sub-teams to ensure delivery at multiple levels of the development team. Design, implement, and optimize effective communication within and outside the team.

Coordinate with corporate communications to lead the team's external communication plan. Ensure the team has a good information management system in line with AZ best practice. Ensure integrity of information management systems to connect to external parties.

Drive continuous improvement in how the team approaches information management Ensure data quality as per agreed standards and monitoring metrics Identify development opportunities for team members Governance and Investment Decisions Lead team towards optimized governance decisions - e.g. evaluate multiple strategic options and drive team to value-maximizing drug development decisions Provide guidance to both the team and senior management / governance bodies that allows efficient (timely and informed) decision making Leverage broad influential network and ensures engagement at all levels prior to key decisions Planning, Monitoring and Delivery Ensure that overall GPT deliverables, budgets, schedules, and performance standards are realistically set, governance approved and attained, and that the project effectively fulfils all information management and business reporting requirements Direct project support staff in maintaining plans of the highest data quality, accountable for all integrated project management deliverables associated with the GPT Accountable for all integrated Project Management deliverables associated with the program Entrepreneurship Serve as a role model for cross-functional collaboration and effective conflict resolution Lead by example in learning and innovation, seek opportunities to change paradigms and remove barriers within and outside the team Apply extensive business insight to drive cross project learning, champion and embed better ways of working across the enterprise. Proactively promote learning and knowledge sharing

Expected to mentor or supervise other project managers. May provide input for staff development, recruitment, succession planning and resource model. Help establish new company best practices Share lessons learned and communicate those throughout the GPM community to drive adoption of knowledge beyond the GPT Essential for the role Bachelor's degree in a scientific or business related field Minimum of 10 years of relevant experience with cross-functional drug development teams.

Extensive experience leading drug development projects including success in multiple roles/development phases/TAs related to drug development project or program management. Track-record of expertly navigating governance processes to drive complex projects forward. Successful track record of delivering complex/ high strategic business impact projects within agreed time, quality and cost.

Expert knowledge of project management tools and processes. Experience of driving cross portfolio, above-asset DA or TA drug development projects. Experience in developing Business Development business cases including pressure testing of proposed timelines, and where applicable, Due Diligence activities.

Skilled at building, motivating, leading and inspiring high performing teams. Proven ability to develop and educate team members and mentor individuals within and outside own function. Experience in project control, project reporting and ensuring high quality project data (milestone, cost, risk) in enterprise systems.

Track record of effective senior stakeholder management, demonstrating effective communication skills and strong ability to influence strategically using data. Desirable for the role Late stage drug development experience Relevant therapeutic area expertise - CVRM and/or Respiratory & Immunology, and/or cell therapy experience. Strong internal network with experience in AZ ways of working.

Track-record of building diverse, inclusive teams and delivering in multi-cultural environments. Office Working Requirements 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. The annual base pay for this position ranges from $206,993.60 - 310,490.40 USD. 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. Ready to make a difference. Apply now and join us on this exciting journey

#LI-Hybrid Date Posted 27-Aug-2026 Closing Date 09-Sept-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In 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.


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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB