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About the Role

Serve as a critical member of project teams by providing analytical insight, leadership, and creativity to client engagements, business development efforts, and internal initiatives. Help define projects, build work plans, and develop valuable conclusions and recommendations for clients in the high-growth Clinical Outcome Assessment (COA) team.

Responsibilities

• Contribute to projects focused on the development, evaluation, and implementation of COA research including Patient Reported Outcomes (PROs).
• Provide research support in all aspects of project delivery including qualitative and quantitative data collection, data analysis, report writing, and writing abstracts and manuscripts.
• Develop qualitative and quantitative research study protocols and associated documents.
• Conduct literature and instrument reviews.
• Plan and conduct reviews of relevant COA/PRO instruments.
• Plan and conduct competitor landscaping activities.
• Plan and conduct qualitative interviews/focus groups.
• Report writing and delivery of findings.
• Distil key messages from data analysis and write recommendations.
• Attend and present at client meetings.
• Attend training as required.
• Work with project team to meet project deadlines and achieve project objectives.
• Effective and timely administration.

Requirements

• A master’s degree in health psychology, psychology, sociology, life sciences or other relevant topic (a 2:1 or higher).
• Experience in qualitative and quantitative research methods.
• Proven experience in MS office suite including Excel, PowerPoint, and Word.
• At least 6 months experience working in a team (either vocational or academic).
• Excellent verbal and written communication.
• Ability to work on multiple projects and prioritize workload.
• Good time management and organizational skills.
• Attention to detail.
• Hard-working with a commitment to high-quality deliverables.
• Ability to work within a team.
• Ability to work proactively and on own initiative and actively solve problems when required.

Skills

• Qualitative research methods
• Quantitative research methods
• MS Office Suite
• Excel
• PowerPoint
• Word
• Verbal communication
• Written communication
• Project prioritization
• Time management
• Organizational skills
• Attention to detail
• Proactive problem-solving

Location

• London, UK

Work Type

• Hybrid
• Full-time
• Permanent

Experience Level

• Associate

Education Level

• Master's degree

Benefits

• Private Medical Insurance or Health Cash plan
• Generous Pension Plan contribution rates
• Income protection insurance
• Life insurance
• Sports Club Subsidy
• Emergency Childcare or Adult care cover
• Eyecare vouchers
• 25 Days Annual Leave + 8 Bank Holidays
• Option to buy and sell Annual leave

About the Company

• 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.

Equal Opportunity

• 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.