Director, Patient Centered Science, Late CVRM

The  Patient Centered Science (PCS) Director leads  therapy area and project-level patient-centered evidence strategies , with a focus on  clinical outcome assessments (COAs) ,  patient-reported outcomes (PROs) , and broader  patient experience data across the product lifecycle.

The role ensures that patient-centered evidence is  fit for purpose and supports  regulatory approval ,  HTA/reimbursement needs , and  commercialization . 

The role holder partners with cross-functional teams to define the most appropriate  COA/PRO endpoints , identify evidence gaps, and recommend or develop instruments and methods that capture the patient experience and meet stakeholder expectations. They provide strategic leadership from early development through late-stage programs, ensuring that patient-centered evidence is integrated into  clinical plans ,  TPPs/TPCs ,  regulatory discussions , and  submission dossiers . 

The PCS Director is accountable for leading  patient input activities , including interviews and related evidence-generation approaches, and for translating those insights into scientifically robust recommendations. The role also represents PCS in interactions with  regulatory authorities ,  HTA bodies , external experts, and internal governance teams, while supporting payer evidence needs such as  utility and  patient preference measurement . 

In addition, the PCS Director drives consistent TA-level standards for PRO/COA strategy, oversees relevant vendors and subprojects, contributes to scientific communications and publications, and strengthens AstraZeneca’s external reputation in  patient-centered measurement science . 

Key Responsibilities

• Lead PCS strategy for assigned therapy area(s) and projects, covering  COA ,  PRO , and  patient experience evidence needs across development. 

• Advise teams on endpoint strategy , including selection, development, validation, and implementation of fit-for-purpose instruments. 

• Identify evidence gaps and define plans to generate robust patient-centered evidence for regulatory, payer, and clinical decision-making. 

• Provide input to clinical development plans ,  TPPs/TPCs , protocols, briefing books, and regulatory submission packages. 

• Lead PCS regulatory and HTA interactions related to PRO/COA evidence and support market access evidence needs where relevant. 

• Generate patient insight through interviews and other research approaches to inform strategy and documentation. 

• Partner cross-functionally with R&D, Medical, Payer, Regulatory, and external experts to align evidence plans and messaging. 

• Manage external vendors and subprojects , including scope, budget, timelines, quality, and deliverables. 

• Drive scientific communication , including presentations, publications, and external engagement to advance AZ’s leadership in PCS. 

Minimum Requirements

• Bachelor’s degree in a clinical, biological, social science, or related field. 

• Master’s degree in outcomes research, epidemiology, health services research, health policy, or a related discipline. 

• Doctoral degree MD preferred . 

• At least 5 years’ experience in the biopharmaceutical industry. 

• Demonstrated experience in  COA/PRO or broader  patient-centered science . 

• Strong understanding of  clinical development ,  study design , and  evidence interpretation . 

• Knowledge of  qualitative and quantitative methods relevant to patient insight and outcome measurement. 

• Experience working across functions and with  external vendors/agencies . 

Skills and Capabilities

• Deep expertise in  PRO/COA strategy and its application in pharmaceutical development. 

• Strong understanding of  global regulatory ,  HTA , and product development requirements. 

• Ability to translate patient-centered evidence into  strategic recommendations and actionable development plans. 

• Strong scientific leadership, problem-solving, and stakeholder management skills. 

• Excellent communication, collaboration, and influencing skills. 

• High integrity and strong ethical standards. 

Key Interfaces

The role works closely with  R&D project teams,  Regulatory ,  Payer and Evidence teams , external consultants, academic partners, and  regulatory/HTA authorities . 

The annual base salary for this position ranges from $194,147.00 to $291,220.00. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).

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.

AstraZeneca offers an environment where you can make a positive impact while building a long-term career filled with global opportunities. Our commitment to delivering accelerated growth pushes us to innovate continuously. With a focus on Lean processes, cutting-edge science, digitalization, and sustainable practices, we are dedicated to making people's lives better. Our inclusive community supports each other on our journeys, fostering curiosity and problem-solving. Embrace the chance to broaden your knowledge and skills in a place where your dedication is rewarded.

Ready to take on this exciting challenge? Apply now to join us in shaping the future of manufacturing technology at AstraZeneca!

Date Posted

Closing Date

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.