Pharmaceutical consultant Work, Jobs in Beaconsfield, Bkm (with Salaries)

Consultant (Clinical Outcome Assessment - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Gym membership
3d
Sr Industry Consultant - AstraZeneca
SAS —Marlow
- Hybrid work
- Bachelor's degree
- Travel
- Computer networking
Associate Consultant (UK) - Entry-Level Technology Consulting (Life Sciences)
Veeva Systems —London
- £40,000 a year
- Full-time
- Hybrid work
- English
- Travel
- Communication skills
Head, PV and Regulatory QA
CSL Seqirus —Maidenhead
- Full-time
- Customer service
- Bachelor's degree
- Organisational skills
Consultant
Prescient Healthcare Group —London
- Full-time
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Quick apply
3d
Senior Principal Biostatistician
Novartis —London
- Full-time
- Doctoral degree
- English
- Communication skills
Account Manager | Healthcare
Health & Tech —London
- Full-time
- Analysis skills
- Annual leave
Quick apply
2d
Pharmaceutical Project Manager
British Compliance Institute —London
- Flexible schedule
QA/GMP Compliance Expert
British Compliance Institute —London
- Flexible schedule
Vice President (Life Sciences Strategy Consulting, Pharma Practice)
BGBx Consulting —London
- Data analysis skills
- Business development
- Bachelor's degree
- Annual leave
- Life insurance
Quick apply
Manufacturing Operations Consultant - London
Chartwell —London
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
Quick apply
Continuous Improvement Expert
British Compliance Institute —London
- Continuous improvement
- Flexible schedule
Regulatory Consultant - CMC (CMC with small molecule products)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
Lead Consultant - Systematic Reviews & Evidence Synthesis
ICON Plc —Reading
- Full-time
- Management
- Doctoral degree
- Master's degree
- Employee assistance programme
10d
Associate Technical Consultant (UK) - Entry-Level Consulting (Life Sciences)
Veeva Systems —London
- £40,000 a year
- Full-time
- Hybrid work
- Azure
- Computer Science
- Java
MHRA AI Regulatory Specialist – 5 day Contract across 8 weeks (Consultant II)
UST —London
- Machine learning
- AI
- Communication skills
Quick apply
12d
Senior Learning Strategy Consultant
サイネオス・ヘルス —London
- Microsoft Powerpoint
- Travel
4d
Management Consultant - Principal - Life Sciences
Moorhouse Consulting —London
- £105,000 a year
- Hybrid work
- IT
- Annual leave
- Employee discount
Head of/Director, Government Affairs - UK & EU
Hims & Hers —London
- £140,000 - £155,000 a year
- Full-time
- Hybrid work
- Spanish
- AI
- Communication skills
- Annual leave
10d
Senior Implementation Consultant
Fusion Risk Management —London
- Full-time
- Salesforce
- Microsoft Office
- Bachelor's degree
Quick apply

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Consultant (Clinical Outcome Assessment - COA)

Clarivate -
London

Apply Now

Job details

Full-time
3 days ago

Benefits

Annual leave
Company pension
Private medical insurance
Gym membership
Life insurance

Qualifications

Microsoft Powerpoint
Report writing
Microsoft Outlook
Doctoral degree
Sociology
Microsoft Office
Master's degree
Psychology
FDA regulations

Full job description

We are looking for a Consultant (Clinical Outcome Assessment - COA) - (UK fully Remote or London Hybrid ) to serve as a critical member of project teams by providing analytical insight, leadership, and creativity to billable client engagements, business development efforts, and internal initiatives.

The Consultant will help define projects, build work plans, and develop robust and valuable conclusions and recommendations for our clients. Consultants are vital to ensuring that we provide our clients with the insights and information they need to achieve success.

This role is focused in a high-growth area of the consulting business; the Clinical Outcome Assessment (COA) Team. You will be expected to:

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

About You – Experience, Education, Skills, and Accomplishments:

A 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.

Preferred Qualifications:

A PhD or PostDoc research experience.
Understanding of clinical drug development and regulatory (FDA, EMA) procedures and guidance.
Knowledge of the pharmaceutical/medical device industry and the clients' operating environment.

What You Will Be Doing:

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.

About the Team:

Our team consists of 30+ outcomes researchers who have extensive methodological and commercial experience. We are experienced in the design, validation, and implementation of PRO measures and other COA instruments for clinical trials and clinical practice, with a focus on FDA, EMA, and HTA bodies. We have significant experience across a range of therapy areas, such as rare disease, oncology, immune disorders, respiratory, psychiatry, CNS, autoimmune, infectious diseases, pain, and women's health. Supported by a global multi-disciplinary team from the wider Clarivate team, we can involve medical writers, health economists, systematic reviewers, and strategic advisors in our projects as needed. Together, our experts provide integrated health economics and outcomes research (HEOR) and market access solutions across the product life cycle.

Hours of Work

This is a full-time position and can be Fully remote in the UK or Hybrid based in London, UK working in our Liverpool Street office (2-3 days per week in office, rest of week remote).

This position requires weekday (Monday - Friday) attendance with some scheduling flexibility available around core working hours.

Our UK Employee Benefits include :

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
From 25 Days Annual Leave + 8 Bank Holidays (option to buy and sell Annual leave)

#LI-Remote, #LI-Hybrid #LI-SK1

At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

Apply Now

Refine Your Search

pharmaceutical consultant jobs in beaconsfield, bkm

Consultant (Clinical Outcome Assessment - COA)

Sr Industry Consultant - AstraZeneca

Associate Consultant (UK) - Entry-Level Technology Consulting (Life Sciences)

Head, PV and Regulatory QA

Consultant

Senior Principal Biostatistician

Account Manager | Healthcare

Pharmaceutical Project Manager

QA/GMP Compliance Expert

Vice President (Life Sciences Strategy Consulting, Pharma Practice)

Manufacturing Operations Consultant - London

Continuous Improvement Expert

Regulatory Consultant - CMC (CMC with small molecule products)

Lead Consultant - Systematic Reviews & Evidence Synthesis

Associate Technical Consultant (UK) - Entry-Level Consulting (Life Sciences)

MHRA AI Regulatory Specialist – 5 day Contract across 8 weeks (Consultant II)

Senior Learning Strategy Consultant

Management Consultant - Principal - Life Sciences

Head of/Director, Government Affairs - UK & EU

Senior Implementation Consultant

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