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Consultant, Clinical Outcome Assessment – COA
ClarivateConsultant leading clinical outcome assessment projects focused on research and analysis in the pharmaceutical sector. Driving strategic insights and client satisfaction with regulatory compliance.
About the role
Key responsibilities & impact- Lead projects focused on the development, evaluation, and implementation of COA research including Patient Reported Outcomes (PROs)
- Provide and drive research activities in all aspects of project delivery including qualitative and quantitative data collection, data analysis, report writing, and writing abstracts and manuscripts
- Lead complex, global COA projects—including the selection, development, and validation of COA instruments such as PRO measures—ensuring alignment with regulatory requirements (e.g., FDA PRO Guidance, EMA, PFDD)
- Provide strategic oversight and scientific direction across multiple concurrent COA engagements, ensuring methodological rigour, high-quality deliverables, and strong client satisfaction
- Drive strategic input into clinical development programmes by guiding clients on COA strategy, endpoint selection, and evidence generation to support labelling claims and market access
- Oversee the design and delivery of mixed-methods research, including concept elicitation and cognitive debriefing interviews, quantitative validation studies, and literature/instrument reviews
- Serve as scientific lead for key client engagements—presenting findings, guiding discussions, and acting as a trusted advisor on COA-related decisions
- Mentor and line-manage associate consultants and associates, providing training in qualitative and quantitative COA methods, regulatory guidance, and the development of endpoint strategies
- Collaborate with internal and external stakeholders (biostatistics, regulatory, clinical teams) to integrate COA strategies into broader clinical and commercial objectives
- Lead business development activities including proposal development, bid defence meetings, and identification of new client opportunities within the COA space
- Contribute to the evolution of the COA practice through thought leadership (e.g., publications, conference presentations), methodology development, and refinement of internal best practices
- Support strategic planning and resource management within the practice, helping to shape team structure, resourcing, and future capabilities
Requirements
What you’ll need- Master’s degree in health psychology, psychology, sociology, life sciences, or another relevant topic (a 2:1 or higher)
- 5 years of experience in outcomes research, qualitative research, and/or patient-reported outcomes development and evaluation
- Proficient with MS Office Suite (PowerPoint, Excel, Word, Outlook, Teams)
- Proficient with qualitative analysis software (e.g., NVIVO, ATLAS, or MAXQDA), qualitative research methods, and literature review methods
- A PhD or PostDoc research experience (preferred)
- Understanding of clinical drug development and regulatory (FDA, EMA) procedures and guidance
- Knowledge of the pharmaceutical/medical device industry and the clients' operating environment
Benefits
Comp & perks- Private Medical Insurance or Health Cash plan
- Generous Pension Plan contribution rates
- Income protection insurance
- Life insurance
- Sports Club Subsidy (Company pays 50% of gym membership, or up to £500)
- Emergency Childcare or Adult care cover
- Eyecare vouchers
- 25 Days Annual Leave + 8 Bank Holidays (option to buy and sell Annual leave)
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Outcomes ResearchData AnalysisReport WritingMixed-Methods ResearchQualitative Analysis SoftwareLiterature Review MethodsEndpoint Strategy DevelopmentStatistical AnalysisProject ManagementClinical Development Knowledge
Soft Skills
MentoringClient EngagementStrategic OversightCollaborationCommunication
Certifications
Master’s Degree in Health PsychologyPhD or PostDoc Research Experience