Project Management Associate Director, Market Access - EU/MENA

Company Overview
ImmunityBio is a vertically integrated commercial stage biotechnology company developing next-generation therapies that bolster the natural immune system to defeat cancers and infectious diseases. The Company’s range of immunotherapy and cell therapy platforms, alone and together, act to drive and sustain an immune response with the goal of creating durable and safe protection against disease. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response. The Company is applying its science and platforms to treating cancers, including the development of potential cancer vaccines, as well as developing immunotherapies and cell therapies that we believe sharply reduce or eliminate the need for standard high-dose chemotherapy. These platforms and their associated product candidates are designed to be more effective, accessible, and easily administered than current standards of care in oncology and infectious diseases.

• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.

• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.

• Work with a collaborative team with the ability to work across different areas of the company.

• Ability to join a growing company with professional development opportunities.

Position Summary

The Project Management Associate Director, Market Access - EU/MENA will coordinate and contribute to the planning, execution, and delivery of global and/or regional market access strategies. This role will establish and oversee cross-functional alignment across health economics (HEOR), pricing, regulatory, medical and commercial teams to secure timely patient access, reimbursement, and commercial success.

Essential Functions

• Define, build, and maintain comprehensive global cross-functional project plans, timelines, and milestones for reimbursement and Health Technology Assessment (HTA) submissions.
• Facilitate meetings and manage workflows between HEOR, Medical Affairs, Regulatory, Pricing, and Commercial teams to ensure seamless data and dossier readiness.
• Drive cross-functional collaboration across HEOR, Medical Affairs, Regulatory, Pricing, and Commercial teams to ensure alignment with global regulatory strategy, business priorities, and product development objectives.
• Proactively identify bottlenecks, regulatory delays, or evidence gaps, and develop contingency plans to keep launch timelines on track.
• Monitor project-related budgets, contract tracking, and external vendor/consultancy deliverables.
• Provide clear, high-level status updates, dashboard metrics, and risk assessments to senior leadership and steering committees.
• Author, review, revise, and maintain Standard Operating Procedures (SOPs), work instructions, regulatory processes, and standardized templates to ensure consistency, and adherence to applicable regulatory requirements.
• Perform ad-hoc and cross-functional duties and/or projects, as assigned, to support business needs and provide developmental opportunities.

Education & Experience

• Bachelor’s degree in Life Sciences, Public Health, Pharmacy, Business, or a related field.
• 5+ years of project management experience specifically within pharma, biotech, medical devices, or healthcare consulting.
• US and ex-US market experience required
• PMP (Project Management Professional) certification is highly preferred.
• Market Access experience highly preferred

Knowledge, Skills, & Abilities

• Strong foundational understanding of the pharmaceutical product lifecycle, global healthcare systems, HTA processes, and reimbursement requirements.
• Proficiency in project management software (e.g., Smartsheet, MS Project, Asana, or Jira).
• Exceptional verbal and written skills to translate complex technical/scientific timelines into clear business actions.
• Proven ability to collaborate with and guide cross-functional, senior experts toward shared milestones.
• Comfort navigating highly fluid environments and evolving regulatory landscapes.

• Maintain corporate confidentiality at all times.

• Detail oriented, with solid organization and time management skills

• Sound judgment, problem solving, matrix management, and collaboration in selecting methods and techniques for obtaining solutions to problems.
• Ability to work effectively with cross-functional teams in a highly matrixed organization.

Working Environment / Physical Environment

• This position works on site remotely as noted in the offer letter.
• Regular work schedule is Monday – Friday, within standard business hours. Flexibility is available with manager approval.
• This position may need to sit for long periods of time and use various computer programs.

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate’s qualifications, prior experience as well as geographic location.

$110,500 (entry-level qualifications) to $120,000 (highly experienced) annually

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio uses artificial intelligence (AI) tools to assist with sourcing and identifying potential candidates for open positions. These tools help us reach qualified applicants and improve the efficiency of our recruitment outreach. No preference is given to applicants sourced or identified by AI tools.

Important: AI is not used to screen, evaluate, rank, assess, or make hiring decisions about applicants. All applications are reviewed by human recruiters and hiring managers. Hiring decisions are made solely by ImmunityBio personnel without automated decision-making.

We are committed to equal employment opportunity and ensure that all candidates are assessed based on their qualifications, skills, and experience through human review.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day • We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.