Senior Director, Patient Centered Science

AstraZeneca plc; Gaithersburg (MD); Hybrid; USD 234,000 - 350,000; Full time

Benefits offered by this job

Qualified retirement programs

Paid time off (vacation/holiday/leaves

Health, dental, and vision coverage

Job summary

AstraZeneca plc is seeking a senior leader to direct Patient Centered Science (PCS), shaping PRO/COA strategies across portfolios, and aligning patient outcomes with regulatory and payer expectations.

You will guide methodological innovation, enable cross-functional integration, and participate in high-level external collaborations to advance patient-focused evidence.

Qualifications

• Advanced degree in outcomes research, health services research, epidemiology, health policy, or related field.
• Minimum 8+ years relevant experience; 5+ years in biopharma; 5+ years PRO/COA.
• In-depth PRO/COA knowledge for regulation, reimbursement, and global contexts.
• Proven experience building and executing patient-centered science strategies.
• Strong regulatory environment understanding affecting development plans and labeling.

Responsibilities

• Lead PCS Directors; develop a high-performing, inclusive team culture.
• Oversee performance and development of direct reports with clear objectives.
• Governance and cross-functional reviews to align PCS outputs with regulatory needs.
• Provide scientific coaching and mentor leaders to build expertise.
• Collaborate with R&I leadership to shape functional strategy and decisions.
• Represent AstraZeneca in external venues (FDA/EMA/HTA) and ensure PCS visibility across development.

Skills

PRO/COA expertise

Cross-functional leadership

Regulatory knowledge

Clinical development insight

RWE methods (DHT)

Staff coaching

Education

MSc/MD/PhD/PharmD

Job description

Location: Gaithersburg, MD

Hybrid: 3 days a week on site

At Patient Centered Science (PCS), our mission is to identify, measure, understand, and communicate meaningful patient outcomes and experiences of their disease and treatment. Our vision is to positively impact lives by amplifying the patient voice in healthcare decision-making. Using qualitative and quantitative methods and research, PCS supports patient-focused drug development by identifying what matters from a patient perspective, and by selecting, modifying, or developing Patient Reported Outcomes (PRO) and other Clinical Outcome Assessments (COA) to serve the needs of patients, regulators, payers, and healthcare professionals.

Accountabilities and Responsibilities

Team Leadership and Line Management

• Lead, manage, and develop a team of PCS Directors, fostering a high-performing, inclusive, scientifically rigorous and innovative team culture.
• Manage the performance and individual development of direct reports through clear individual objectives and development plans.
• Provide oversight of project support and scientific deliverables; and participate in governance bodies and senior cross-functional reviews, ensuring that PCS strategies and outputs across the portfolio are aligned with regulatory, payer, and patient requirements.
• Provide technical and scientific coaching to direct reports through leadership review of deliverables, helping to build expertise and confidence across the team.
• Working with R&I clinical development leadership teams, contributing to functional strategy, capability priorities, and operational decision-making.
• Serve as a senior point of contact for cross functional R&I colleagues ensuring PCS is well-integrated and influential at all stages of development, and aligning PCS strategy, knowledge and experience sharing across BioPharma.

Scientific and Strategic Leadership

• Set and drive PCS strategy at therapeutic area and portfolio level, ensuring the patient experience of disease and treatment is a central consideration throughout drug development.
• Provide direct project support by: leading all aspects of the development and delivery of PRO/COA strategies and evidence generation plans – including patient experience research, instrument selection or development, and endpoint strategies – to meet the needs of regulators, payers, and patients.
• ensuring PCS contributions are effectively embedded in clinical development through cross-functional collaboration, and that PCS expertise informs clinical study design, governance documents, and results interpretation.
• supporting regulatory and HTA interactions related to PRO/COA, ensuring robust evidence dossiers and a consistent, credible external position.
• Drive methodological innovation and standard process across the team, championing innovative approaches to collecting and communicating patient experience both within AstraZeneca and in the broader scientific community.
• Disseminate PCS-related evidence in scientific publications, internal and external presentations (eg posters and presentations at congresses), and in lay summaries to patients and other stakeholders
• Represent AstraZeneca at critical external venues and collaborations, including interactions with the FDA, EMA, industry PRO consortia, and HTA bodies.

Essential Requirements

• Advanced degree (MSc, MD, PhD, PharmD) in a relevant field such as outcomes research, health services research, epidemiology, health policy, or a related discipline.
• Minimum of 8+years of relevant experience, including at least 5 years in the biopharmaceutical industry and at least 5 years of dedicated PRO/COA experience.
• In-depth expert knowledge of PRO/COA and its application to pharmaceutical development, regulatory approval, and reimbursement at an international level.
• Proven experience of developing and implementing patient-centered science strategies at project, therapeutic area, and portfolio level.
• Strong knowledge of regulatory environment influencing clinical development plans, labeling, and promotional claims.
• Excellent knowledge of clinical development, research study designs, and their interpretation.
• Experience of managing, coaching, and developing scientific staff in a complex, matrixed organization.
• Experience of cross-functional collaboration and influencing without authority at senior levels.
• Understanding and background in digital health technology (DHT) real-world evidence (RWE) methods and their application alongside clinical development.

Desirable

• Doctoral degree (PhD or equivalent) in a relevant field.
• Experience of PRO instrument development and validation and PRO dossier generation, including successful negotiations with regulatory authorities.
• Experience of working within respiratory and immunology therapeutic areas.
• Participation in external partnerships, industry consortia, or academic collaborations in patient-centered science.
• Experience of direct interactions with regulatory and health agencies (e.g., FDA, EMA) and HTA bodies.

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering groundbreaking methods, and bringing unexpected teams together. Interested? Come and join our journey.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We follow all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

The annual base salary for this position ranges from $233,586.40 - 350,379.60 USD Annual. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, 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.

Date Posted 04-Nov-2026

Closing Date 26-Nov-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.