Senior Research Associate

Senior Research Associate, Patient‑Centered Outcomes

Adelphi Values is a leading health outcomes consultancy that works with a wide range of pharmaceutical companies. The Patient‑Centered Outcomes (PCO) team are global leaders in the selection, development, validation, and use of Patient‑Reported Outcome measures (PROs) and other Clinical Outcome Assessments (COA). We are a dedicated team of researchers proud of our friendly, supportive culture, reputation for high‑quality research, and client service which puts the patient at the centre of drug development.

Our purpose is to improve patients’ lives by informing healthcare decisions. We do this by supporting clients in the selection, development, psychometric validation, and implementation of COAs that form clinical trial endpoints or are used in clinical practice to support the evaluation of the patient experience and assessment of treatment benefit.

• Undergraduate/postgraduate degree (BSc, MSc or similar) in health psychology, psychology, psychological research methods, sociology, or life sciences.
• Minimum 1.5‑2 years of work experience in a related research or health setting or consultancy, with demonstrable evidence of strong independent and self‑driven working.
• Knowledge and experience of literature review methodology, qualitative/quantitative analysis and research design including data collection, analysis, interpretation, and dissemination.
• Fluency in Microsoft Office packages, organisational skills, self‑motivation, and attention to detail.
• Teamwork ethos and appetite for working in a fast‑paced, fun environment.
• Eligibility to work in the UK.

You will join a dynamic team of researchers with a passion for excellence in research and client service. You will have a genuine interest in understanding, evaluating, and communicating the patient perspective. You will have the opportunity to learn about many different health conditions and develop your skills in qualitative, quantitative, and mixed methods research.

• Conduct literature reviews.
• Develop study protocols and statistical analysis plans.
• Prepare study documentation for ethical review.
• Recruit and interview study participants.
• Analyse data.
• Report study findings and write conference abstracts/posters and journal manuscripts.
• Manage multiple projects concurrently.
• Work closely with colleagues based in the UK and/or US.

Competitive salary, performance‑related rewards, health insurance, pension, and on‑site gym membership. Support for training and development and career progression opportunities. Hybrid role based at our head office in Bollington, near Macclesfield – with a minimum of 2 days in office.

Applications from recruitment agencies will not be accepted.

Omnicom Health is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we’re focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us—we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice.