Associate Consultant

1 month ago

London, United Kingdom Clarivate Full time

Associate Consultant (Clinical Outcome Assessment - COA) - London, UK ( Hybrid)

About the Clarivate Consulting team

Clarivate Consulting provides advisory and management consulting services to industry-leading and emerging pharmaceutical, biotechnology and MedTech companies. We combine deep domain expertise and data driven analysis to deliver relevant insights and customized, actionable solutions for our clients in the areas of new product planning, commercial strategy and pricing & market access.

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

This role is primarily focused in two high-growth areas of the consulting business; Clinical Outcome assessment:

- Contribute to projects focused on the development, evaluation, and implementation of Clinical Outcome Assessments research including Patient Reported Outcomes.
- Provide research support 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 other relevant topic (a 2:1 or higher)
- At least 12 months experience in outcomes research, qualitative research and/or patient reported outcomes development and evaluation
- Proven experience in MS office suite including Excel, PowerPoint, and Word
- At least 6 months experience working in a team (either vocational or academic

It would be great if you also have:

- A PHD
- Understanding of clinical drug development and regulatory (FDA, EMA) procedures and guidance
- Knowledge of the pharmaceutical/medical device industry and the clients operating environment
- Excellent verbal and written communication
- Proven experience in Atlas, NVIVO or MAXQDA
- Ability to work on multiple projects and prioritise workload
- Good time management, organisational skills, and attention to detail
- Hard-working with a commitment to high-quality deliverables
- Ability to work proactively and on own initiative and actively solve problems when required

What will you be doing in this role?
- Project Delivery
- Conduct research to produce consistently high-quality deliverables with mínimal guidance including:

- Develop qualitative and quantitative research study protocols including interview guide development, and survey development
- Lead and conduct literature and instrument reviews including development of search strategy protocols, citation screening, literature review, development of data extraction tables, and review of social media data where appropriate
- Plan and conduct reviews of relevant COA/PRO instruments according to scientific and regulatory guideline
- Plan and conduct competitor landscaping activities e.g., review of PROLabels, clinicatrials.gov, EPARs, approved FDA and EMA labels, and regulatory meeting minutes and communications
- Plan and conduct qualitative interviews/focus groups with patients, clinicians, caregivers, and other relevant stakeholder groups
- Provide research guidance and advice to research analysts
- Report writing and delivery of findings (Word/PowerPoint)
- Distill 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 (conform to house styles and processes)

About the Team:
Our team consists of 18 health psychologists and outcomes researchers by training who have extensive methodological and commercial experience.

Experienced in the design, validation, and implementation of patient-reported outcome (PRO) and other COA instruments for clinical trials and clinical practice, with a focus on FDA and EMA, and HTA bodies with Significant experience across a range of Therapy areas, such as 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 permanent position based in London, UK and will require hybrid working in our Liverpool Street off

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