Gaithersburg, Maryland, United States
Onsite
WHY JOIN US?
Evinova is a health-tech business, accelerating the delivery of better health outcomes by propelling the life sciences sector forward in digital health, from the inside. Through our application of science-based expertise, evidence-led rigour, and human insight, our digital solutions are deliberately designed so that everyone can reach better health outcomes together. Evinova is a health-tech business within the AstraZeneca Group.
Digital health, the point at which healthcare, technology, data and analytics converge, is the subject of phenomenal promise, with the World Health Organisation believing it has the potential to improve health for everyone. At AstraZeneca, we’ve been working hard to make this a reality, with the years of experience we have accumulated enabling us to now embed digital health at scale across R&D.
To achieve our goal of improving patient experience and outcomes AstraZeneca has Digital Health as one of the top 4 strategic priorities for the company, details on digital health strategy can be found here. Oncology is the largest therapeutic area within AstraZeneca and second highest cause of death globally, with AstraZeneca’s ambition to eliminate cancer as a cause of death.
Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.
About the Opportunity:
If you’re passionate about advancing oncology drug development, consider joining us as a Senior Scientist in Clinical Outcomes Assessment (COA) Measurement Science. In this role, you’ll apply your knowledge of clinical outcomes assessments and emerging sensor or wearable data collection technologies to drive meaningful insights.
Your contributions will help shape the understanding and measurement of symptoms, functional outcomes, health-related quality of life, and other patient-focused aspects at every stage of the oncology drug development process. You’ll offer both qualitative and quantitative expertise to support patient-centered measurement strategies. Working closely with stakeholders, you’ll play a key role in identifying and balancing treatment benefits and risks in Oncology.
Accountabilities:
As the Senior Scientist, you will play a pivotal role in channelling our scientific capabilities to make a positive impact on changing patients’ lives through the following:
Contribute to qualitative and quantitative research to generate evidence of patients' experience with treatment throughout the oncology drug development lifecycle (e.g., identification and exploration of unmet measurement need, endpoints capturing symptoms, function, or quality of life evolution overtime to inform disease progression or tolerability) including study design/oversight and data collection
With supervision, responsible for project management of functional service provider(s) for qualitative and quantitative research to inform development of conceptual disease-models and related endpoints to address measurement gap to inform the patients' experience with treatment.
With supervision, contribute to the exploration of COA in clinical research to inform clinical benefit evaluation of oncology treatment, including: measurement performance evaluation of symptom(s), function and health-related quality of life instruments, definition or development of novel COA endpoints to address evidence needs from key stakeholders, and data collection to inform decision making related to the inclusion of COA endpoints and findings in major deliverables such as: clinical development plans, study protocols, and strategic and operational reports.
With support from line management, partner with scientific leaders within Digital Health Oncology to identify, pursue, and develop independent scientific expertise within the COA and digital health fields.
Collaborate and partner with key internal stakeholder colleagues to ensure priorities and strategies are aligned.
Prepare, review, and publish scientific reports, internal/ conference presentations, publications, regulatory dossiers reflecting ongoing or completed work, with supervision.
Essentials Skills and Experience:
Minimum of a Bachelor's degree in a related field, and four years practical experience is required.
An advanced degree in a science related field and/or other appropriate knowledge/experience is preferred. Combination of academic training and practical experience in outcomes research is highly preferred: Doctoral degree (e.g., Ph.D., Sc. D. or Dr.P.H.) in a relevant field such as, but not limited to, health services research, health outcomes research, epidemiology, pharmacy administration, public health, economics, statistics or decision sciences or Clinical degree (e.g., in medicine, pharmacy, nursing, or equivalent) and a masters degree in a related field (as noted above), plus two years practical experience or: Masters degree in a related field (as noted above), plus two years practical experience
Experience in performing outcomes research, in any setting, including life sciences company, research organization, academic institution or governmental agency, including experience in interpreting COA data from clinical research and communicating scientific evidence.
Experience conducting literature reviews
Working knowledge of Patient Focused Drug Development (PFDD) FDA Guidance documents and other relevant guidance documents and standard processes to capture patient's experience in drug lifecycle
Project management and vendor management skills
Conceptual, analytical and critical thinking
Creative, innovative, solution-focused
Curious, embraces new ways of problem solving, new ideas, and new ways of working
Strong communication skills, the ability to build relationships
Desirable for the Role:
Prior experience conducting outcomes research studies and communication of study findings to internal and external audiences
Quantitative and data analysis experience, particularly with clinical trial data
Experience with the development, selection, and psychometric evaluation of PRO instruments used in clinical studies
Experience conducting qualitative interviews with patients and clinicians and performing qualitative data analysis
Experience conducting outcomes research in different geographic regions and interacting with regulators and policy-makers
Diligence - attention to detail and ability to manage a program of concurrent activities
Resilience - ability to overcome and motivate others in the face of a changing environment
The annual base pay (or hourly rate of compensation) for this position ranges from 115,899.20 to 173,848.80 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.
At AstraZeneca, we believe in the potential of our people, and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As a Statistical Programming Director, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives and join us on an exciting journey to pioneer the future of healthcare.
AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.
Why Evinova (AstraZeneca)?
Evinova draws on AstraZeneca’s deep experience developing novel therapeutics, informed by insights from thousands of patients and clinical researchers. Together, we can accelerate the delivery of life-changing medicines, improve the design and delivery of clinical trials for better patient experiences and outcomes, and think more holistically about patient care before, during and after treatment. We know that regulators, healthcare professionals and care teams at clinical trial sites do not want a fragmented approach. They do not want a future where every pharmaceutical company provides their own, different digital solutions. They want solutions that work across the sector, simplify their workload and benefit patients broadly. By bringing our solutions to the wider healthcare community, we can help build more unified approaches to how we all develop and deploy digital technologies, better serving our teams, physicians and ultimately patients. Evinova represents a unique opportunity to deliver meaningful outcomes with digital and AI to serve the wider healthcare community and create new standards for the sector. Join us on our journey of building a new kind of health tech business to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey.
So, what’s next! (select one Call to Action -CTA text)
Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.
Date Posted
06-Jul-2026Closing Date
19-Jul-2026Our 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.
Want to know if this job is worth applying to?