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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 robust conclusions and recommendations for clients, focusing on 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.
• Conduct research to produce consistently high-quality deliverables.
• 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 with patients, clinicians, caregivers, and other relevant stakeholder 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

• 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 and quantitative research methods
• MS office suite including Excel, PowerPoint, and Word
• Outcomes research and/or patient-reported outcomes development and evaluation (desired)
• Understanding of clinical drug development and regulatory (FDA, EMA) procedures and guidance (desired)
• Knowledge of the pharmaceutical/medical device industry and the client's operating environment (desired)

Location

• London
• UK

Work Type

• Hybrid
• Full-time
• Permanent

Experience Level

• Associate

Education Level

• Master’s degree in health psychology, psychology, sociology, life sciences or other relevant topic (a 2:1 or higher)

Benefits

• 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)

About the Company

• Clarivate is a global leader in trusted and transformative intelligence.
• We bring together enriched data, insights, analytics and workflow solutions, grounded in deep domain expertise across the spectrum of knowledge, research and innovation.
• Our aim is to fuel the world’s greatest breakthroughs by harnessing the power of human ingenuity.
• For more information, please visit clarivate.com

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.