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Health Psychologist and Outcomes Researcher

2 months ago


London, Greater London, United Kingdom Clarivate Full time
About the Role

We are seeking a highly skilled Health Psychologist and Outcomes Researcher to join our team as an Associate Consultant - Clinical Outcome Assessment. This is a critical role that requires expertise in the design, validation, and implementation of patient-reported outcome (PRO) and other Clinical Outcome Assessment (COA) instruments for clinical trials and clinical practice.

Key Responsibilities
  • Conduct research to produce high-quality deliverables with minimal guidance, including developing qualitative and quantitative research study protocols, leading and conducting literature and instrument reviews, and planning and conducting reviews of relevant COA/PRO instruments.
  • Provide research guidance and advice to research analysts, report writing and delivery of findings, and distill key messages from data analysis and write recommendations.
  • Attend and present at client meetings, and attend training as required.
  • Work with project team to meet project deadlines and achieve project objectives, and effectively and timely administer tasks conforming 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. We have a global multi-disciplinary team that provides integrated health economics and outcomes research (HEOR) and market access solutions across the product life cycle.

Requirements
  • 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).
Preferred Qualifications
  • 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.
Working Arrangements

This is a full-time permanent position based in London, UK and will require hybrid 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.

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).