Associate Director, Clinical Outcomes Assessment

2 days ago


Gaithersburg MD United States National Black MBA Association Full time

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.

We’re building out a best-in-class Measurement Science team to support the R&D portfolio as well as digital therapeutics, which will be part of the future of measurement science and analytics to support novel endpoints/interventions.

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.

An Associate Director in the COA Measurement Science, Centre of Excellence should have experience in the use of clinical outcomes assessments (COA) such as traditional survey-like instruments using rating or ranking scales and novel sensor/wearable data capture instruments to inform identification and/or evaluation of symptoms, function, health-related quality of life, or other patient-centric concept of clinical benefit throughout the oncology drug development lifecycle. With supervision, the Associate Director will be responsible for providing qualitative and quantitative measurement support for the development and execution of patient-centered measurement strategy and dissemination of its findings to key collaborators, such as R&D global and/or cross-functional teams, regulators, payers, healthcare professionals and most importantly patients in support of more efficient identification of treatment benefits vs harms in Oncology. This includes but is not limited to: identification and exploration of unmet measurement need by conducting literature reviews and/or qualitative research studies, description of context of use (e.g., selection of responders for fit-for-purpose use of Patient-Reported Outcomes, Observer-Reported Outcomes, Clinician-Reported Outcomes, or Performance Outcome assessments), selection of data collection strategy and implementation in clinical research or real world setting, collaboration for data analyses and interpretation and audience-adapted publications.

What you’ll do

  • Contribute to qualitative and quantitative research to generate evidence of patients' experience with treatment throughout the oncology drug development lifecycle.
  • Responsible for project management of functional service provider(s) for qualitative and quantitative research.
  • Contribute to the exploration of COA in clinical research to inform clinical benefit evaluation of oncology treatment.
  • Partner with scientific leaders within Digital Health Oncology to identify, pursue, and develop independent scientific expertise.
  • Collaborate and partner with key internal collaborator 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.

Essential for the role

  • Combination of academic training and practical experience in outcomes research.
  • Experience in performing outcomes research in any setting.
  • Experience in conducting literature reviews.
  • Working knowledge of Patient Focused Drug Development (PFDD) FDA Guidance documents.
  • Project management and vendor management skills.
  • Conceptual, analytical and critical thinking.
  • Strong communication skills and ability to establish relationships.

Desirable for the role

  • Conducting of outcomes research studies, and the communication of study findings to internal and external audiences.
  • Experience with the development and selection of PRO instruments used in clinical studies.
  • Experience in conducting qualitative interviews with patients and clinicians.
  • Diligence - attention to detail and ability to manage a program of concurrent activities.

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.

Date Posted: 04-Dec-2024

Closing Date: 17-Dec-2024

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