Consultant, Clinical Outcome Assessment – COA

Clarivate

Consultant leading clinical outcome assessment projects focused on research and analysis in the pharmaceutical sector. Driving strategic insights and client satisfaction with regulatory compliance.

Posted 7/1/2026full-timeLondon • 🇬🇧 United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading COA research projects, including the development and validation of Patient Reported Outcomes (PROs), while ensuring compliance with regulatory standards. Proficient in qualitative and quantitative research methodologies, with a strong focus on strategic oversight and client engagement.

Highest-signal resume keywords

COA Research LeadershipPatient Reported Outcomes DevelopmentQualitative Research MethodsRegulatory Compliance (FDA, EMA)Business Development in COA

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Outcomes ResearchData AnalysisReport WritingMixed-Methods ResearchQualitative Analysis SoftwareLiterature Review MethodsEndpoint Strategy DevelopmentStatistical AnalysisProject ManagementClinical Development Knowledge

Soft Skills

MentoringClient EngagementStrategic OversightCollaborationCommunication

Tools & Technologies

MS Office SuiteNVIVOATLASMAXQDAPowerPointExcelWordOutlookTeams

Certifications & Qualifications

Master’s Degree in Health PsychologyPhD or PostDoc Research Experience

Industry Keywords

Pharmaceutical IndustryMedical Device IndustryClinical Drug DevelopmentRegulatory GuidancePatient-Reported Outcomes

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)