Director/Senior Director, Clinical Outcomes Assessment (COA) Strategy, Development & Implementation
Listed on 2026-08-05
-
Science
Clinical Research
Overview
Shionogi is committed to incorporating the voice of the patient into its clinical development programs. The Director/Senior Director of COA Strategy, Development & Implementation is responsible for developing a given asset’s COA strategy to ensure patient‑centered, regulatory‑acceptable, and value‑laden endpoints are incorporated into the development program. This role provides strategic leadership to cross‑functional study teams to ensure COA measures are fit‑for‑purpose to inform patient-physician treatment strategies, health technology assessments, and payers’ willingness to pay.
The successful candidate will have deep subject matter expertise in COA measurement sciences, excellent communication skills, and demonstrated experience in effectively collaborating with cross‑functional colleagues and external suppliers to ensure adoption of strategic recommendations, development of de novo measures as needed, and enabling operational excellence to ensure high‑quality data collection. The position sits within Global Scientific Operations, alongside Healthcare Value and Access, Epidemiology & Real‑world Evidence, and Medical Affairs.
- Engage with assets across the pipeline to identify patient‑relevant concepts, guide asset team’s decision on COA measures that support clinical trials endpoints.
- Determine if COA measures are fit‑for‑purpose for label inclusion; guide the cross‑functional team to assess COAs’ label worthiness based on FDA regulatory guidance (2018‑2023 PFDD guidance documents).
- Conduct landscape assessments to better understand relevant patient concepts of interest and meaningful aspects of health for a given disease area.
- Conduct concept elicitation to identify and/or confirm patient‑relevant concepts of interest and meaningful aspects of health specific to a given disease area.
- Determine whether to use publicly available COA measures as is, modify or develop de novo measures based on COA strategies that will inform necessary claims, support market differentiation, and access‑related decision‑making to improve patient and health system outcomes.
- Conduct cognitive interviews if developing de novo measures.
- Collect patient experience data including conduct embedded clinical trial interviews.
- Engage with regulatory colleagues to complete briefing books to gain FDA guidance on measure development and/or inclusion in clinical trials to ensure measures supporting endpoints will be acceptable for label inclusion.
- Develop and oversee psychometric analysis plans to generate evidence that COA measures used in clinical trials are fit for purpose in the specific context of use.
- Work with clinical operations to ensure data missingness is reduced; that eCOA suppliers have the necessary skill set to effectively implement the COAs that have been included in the protocol and appropriate data reporting is undertaken on a regular basis to ensure quality data is being collected.
- Enable out‑of‑the‑box thinking to enable Shionogi to be an innovator in the area of COA measurement science.
- Participate in relevant conferences and congresses to help establish Shionogi as a COA measurement science innovator.
- Contribute to Shionogi’s COA Center of Expertise (COE) to help deepen and strengthen cross‑functional colleagues’ knowledge of COA measurement sciences and developing market trends.
- Work with colleagues in policy to help inform strategies to further advance the use of patient experience data to help inform access‑related decision‑making and patient care in clinical practice.
Job Requirements
Qualifications
- Masters or PhD in health sciences, psychology, statistics or another related field.
- Requires a minimum of 7 years (Director) or 10+ years (Senior Director) of experience within pharmaceutical industry with responsibility for developing and implementing COA‑related strategies and tactics.
Competencies
- Deep subject matter expertise in COA measurement sciences.
- Strong working knowledge of FDA’s 2018‑2023 PFDD Guidance Documents including market trends.
- Understanding of quality reporting to ensure data collection is consistent within and across measures; that outliers are appropriately…
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).