Clarivate
Consultant (Clinical Outcome Assessment - COA)

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Consultant (Clinical Outcome Assessment - COA)
Consultant (Clinical Outcome Assessment - COA)
UK Fully Remote or London Hybrid
We are looking for a Consultant (Clinical Outcome Assessment - COA) to play a critical role in project teams by delivering analytical insight, leadership, and creativity across billable clients, business development, and internal initiatives.
Role Overview
Coordinates and supports the development, evaluation, and implementation of Clinical Outcome Assessments (COAs), including Patient Reported Outcomes (PROs). This high-growth position focuses on informing strategy, creating robust evidence, and ensuring compliance with regulatory frameworks.
Responsibilities
- Lead COA research projects, encompassing selection, development, and validation of COA instruments.
- Oversee qualitative and quantitative data collection, perform data analysis, and produce comprehensive scientific deliverables (reports, manuscripts, and abstracts).
- Align with regulatory requirements (FDA PRO Guidance, ICH, EMA, or HTA bodies), ensuring methodology adheres to international standards.
- Develop COA strategies and endpoints to support labelling claims, clinical development, and market access.
- Design and execute mixed-methods research, including interviews, cognitive debriefing, and validation studies.
- Provide strategic scientific leadership for high-profile client engagements—advising on project direction, presenting findings, and advising on COA-related decisions.
- Mentor junior colleagues, delivering training in COA methods, regulatory science, and endpoint strategies.
- Collaborate with internal stakeholders (biostatisticians, regulatory teams, clinical experts) and external partners to integrate COA insights into broader initiatives.
- Drive business development, participating in proposals, bid defence meetings, and client outreach within the COA domain.
- Support thought leadership via publications, conference presentations, and best-practice policies to grow the practice.
- Engage in strategic planning by assisting in workforce resourcing and future capability development.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
See breakdownIt searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Requirements
Core Qualifications
- Master’s degree (2:1 or above) in:
- Health psychology
- Psychology
- Sociology
- Life sciences
- Another relevant discipline
- 5 years’ experience in:
- Clinical outcomes research or COA/PRO development
- Qualitative or quantitative research methodologies
- Proficiency with:
- MS Office Suite (Excel, PowerPoint, Word, Outlook, Teams)
- Qualitative research software (NVIVO, ATLAS.ti, MAXQDA) and methods (e.g., literature review, thematic analysis)
Preferred
- Doctoral degree or PostDoc experience
- Strong industry knowledge:
- Clinical drug development and regulatory procedures (FDA, EMA guidance)
- Experience with healthcare regulators or pharmaceutical/medical device sector experience


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About the Team
This is a 30+ member team specialising in COA and PRO validation for:
- Early and late-stage clinical trials
- Regulatory submissions (FDA, EMA, HTA)
- Disease areas: rare disease, oncology, immune disorders, psychiatry, pain, and more
- Multidisciplinary capabilities, with access to integrated health economics, outcomes research, and market access expertise.
The team operates within Clarivate, a global solutions provider combining data intelligence, analytics, and market expertise.
Work Arrangements
- Full-time, hybrid (2–3 days per week in Liverpool Street, London)
- Fully remote (UK-based) alternatives available
- Weekday focus (Mondays–Fridays), with flexible scheduling.
Benefits
Medical & Wellbeing:
- Private Medical Insurance or cash plan benefit
- Generous pension contribution
- Income protection & life insurance
- Sport Club Subsidy (Company covers up to 50% of gym fees or £500)
Work-Life Balance:
- 25+ paid leave days + 8 bank holidays
- Option to buy/sell leave
Support:
- Emergency childcare/adult care coverage
- Eyecare vouchers
Inclusion & Valued Leadership Clarivate fosters equality in recruitment, development, and compensation processes—ensuring all employees have equitable career growth opportunities. The organisation adheres to appropriate nondiscrimination standards.
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