Associate Director, Medical Affairs Operations

Lyell Immunopharma; West Virginia; On-site; USD 180,000 - 230,000; Full time

Job summary

Lyell Immunopharma is seeking an Associate Director of Medical Affairs Operations to build and run the systems, processes, and execution engine for Medical Affairs as the team scales toward commercialization.

The role focuses on operations cadence, budgets, MAVS (MRC), KPIs, and compliance, while enabling AI-powered workflows and cross-functional collaboration across Clinical Development, Regulatory, and Commercial teams.

Qualifications

• 9+ years in Medical Affairs operations or related field
• Experience running congresses, advisory boards, MRC, budgets, KPIs
• Experience with AI adoption in workflows and automation

Responsibilities

• Lead Medical Affairs operations cadence and KPI reporting.
• Manage budgets, contracts, and vendor relationships.
• Plan and execute congresses, advisory boards, and events.
• Implement AI enablement, automation, and dashboards.
• Coordinate with Clinical Development, Regulatory, and Commercial teams.

Skills

Program management

AI tools

Biotech experience

Regulatory knowledge

Cross-functional collaboration

Launch readiness

Education

Bachelor's degree

Advanced degree (MBA/PharmD/PhD/MS)

Tools

CRM systems

Insights platforms

Job description

Job Description

Using living cells to treat – and sometimes even cure – cancer is one of the most dramatic advances in modern medicine. Patients with hematologic malignancies have been successfully treated with cell therapies. However, these profound results have not yet been achieved in patients with solid tumors, representing approximately 90% of all cancers. And for patients with hematologic malignancies, there is a need for next-generation cell therapies that can deliver increased response rates and longer duration of response. We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. Lyell's product candidates are enhanced with novel technology designed to generate T cells that resist exhaustion and have qualities of durable stemness in order to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical response. We were founded by cell therapy pioneers whose decades of research elevated the broader understanding of T-cell biology and its interaction with cancer. In our quest to advance next-generation CAR T-cell therapies, we have built a fully integrated company capable of discovering new technologies, translating science into therapies, manufacturing cell therapy products, and clinically evaluating them in patients. Our culture is based on Science, Respect, Collaboration, and Courage and reflects who we are, the environment we create, and our mission's urgency.

Reporting to the SVP of Medical Affairs, the Associate Director, Medical Affairs Operations is the operational backbone of Lyell's growing Medical Affairs function. As the team scales toward commercialization, this role builds and runs the systems, processes, and execution engine that allow Medical Affairs to operate with speed, consistency, and compliance, spanning scientific congresses and advisory boards, the Materials Review Committee (MRC), field medical support, budget and vendor management, and performance metrics.

KEY ROLE AND RESPONSIBILITIES

Medical Affairs Operations & Business Management

• Establish and run the operating cadence of Medical Affairs: annual and tactical planning, prioritization, and status reporting in partnership with the Head of Medical Affairs and functional leads.
• Support budget planning, tracking, and vendor and contract management for the Medical Affairs function, in partnership with the SVP of Medical Affairs.
• Define and report Key Performance Indicators (KPIs) and metrics that measure the quality, impact, and efficiency of Medical Affairs activities.
• Author and maintain Medical Affairs operating processes and SOPs, ensuring the function is audit-ready and launch-ready.
• Facilitate the Materials Review Committee (MRC); intake, cadence, action tracking, and storage and disbursement of final deliverables.

Congresses, Advisory Boards & Scientific Events

• Plan and execute the operational delivery of scientific congresses, symposia, and advisory boards: logistics, budgets, vendors, contracting, content routing, and compliance in partnership with the medical and field teams.
• Build the calendar, playbooks, and infrastructure that let the team scale event volume without sacrificing quality or compliance as the pipeline advances.

Field Medical Support & Systems

• Support the implementation and day-to-day administration of core Medical Affairs systems (e.g., CRM, insights and content platforms), driving consistent, high-quality use across the team.
• Support field medical infrastructure, onboarding, and enablement as new MSLs are integrated
• Build the reporting and dashboards that turn field activity and insights into decision-ready views for Medical Affairs leadership.

AI Enablement & Digital Ways of Working

• Serve as the AI vanguard within Medical Affairs; identifying workflow pain points and resolving them through targeted, compliant application of AI, automation, and analytics tools.
• Develop use cases, build automations and reusable workflows, and create the shared prompts, skills, and standards that make AI-native work the default across the team.
• Evaluate emerging capabilities and surface those with meaningful, compliant applicability to Medical Affairs.

Cross-Functional Coordination

• Serve as the operational connective tissue between Medical Affairs and the rest of the organization: Clinical Development, Clinical Operations, Regulatory, Commercial, and G&A.
• Coordinate Medical Affairs inputs to launch-readiness workstreams in partnership with cross-functional teams.

Compliance & Governance

• Ensure Medical Affairs activities and systems comply with legal, regulatory, and corporate standards.
• Champion the responsible, compliant adoption of AI and digital tools, maintaining data integrity, confidentiality, and appropriate controls and documentation.

PREFERRED EDUCATION

• Bachelor's degree required; an advanced degree (e.g., MBA, PharmD, PhD, MS, or equivalent) is preferred.
• Familiarity with oncology, hematology, or cell therapy is valued; scientific literacy is an asset given the nature of Medical Affairs work.

PREFERRED EXPERIENCE

• 9+ years of experience in Medical Affairs operations, medical excellence, business operations, or a comparable operations/program management function in the pharmaceutical or biotechnology industry; 5+ for Masters degree, 3+ years for candidates holding a relevant advanced degree, e.g., PharmD or PhD.
• Demonstrated experience operating the core machinery of Medical Affairs; congresses, advisory boards, MRC/review, field support, budgets, and KPIs.
• Demonstrated, hands‑on adoption of AI tools in real workflows, not only sponsoring adoption, but personally building automations, dashboards, or analyses. Deep AI expertise is not required; rapid learning and practical fluency are.
• Track record of building operating processes and systems in a fast‑moving, high‑growth environment with limited infrastructure; launch or launch‑preparation experience is a strong plus.
• Strong working knowledge of U.S. compliance and regulatory requirements applicable to Medical Affairs and HCP interactions.

KNOWLEDGE, SKILLS, AND ABILITIES

• Rare combination of orchestrator and doer; able to move fluidly between designing an operating model and building it.
• Excellent program and project management, organizational, and prioritization skills across multiple concurrent initiatives.
• Strong technical and analytical chops; comfort building with AI, automation, and data tools, and modeling AI‑native ways of working for the broader team.
• Self‑directed operator who identifies problems and proposes solutions without prompting, scoping and launching initiatives with general guidance from senior leadership.
• Exceptional collaboration and influencing skills; operates credibly with medical, field, and cross‑functional leaders.
• High adaptability and comfort with ambiguity in a rapidly evolving, high‑growth biotech environment.
• Strong ethical judgment, integrity, and commitment to compliance and data integrity.
• Passion for transforming patient outcomes through cutting‑edge science and modern ways of working.
• This includes Finance, IT, HR and Legal as systems are built to support in‑field teams. Includes policy and practice as well as systems

The salary range for this position is $180,000 to $230,000, annually, with the opportunity to earn an annual bonus. The salary range is an estimate, and the actual salary may vary based on Lyell's compensation practices and an applicant's qualifications and experience. Employees are also eligible to participate in Lyell's Equity Incentive Plan.

At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees. Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.