Senior Research Manager – Patient Centred Outcomes

Company: Carrot Group
Apply for the Senior Research Manager – Patient Centred Outcomes
Location: Cheshire
Job Description:

Overview

In this role you lead complex PROs and COA-focused research for pharmaceutical clients, shaping measurement strategies and guiding project delivery. You work with cross-functional teams to ensure high-quality, regulatory-aligned evidence that informs clinical development. You’ll manage client relationships, coach junior staff and contribute to business development. This is an opportunity to drive patient-centered outcomes in a globally connected consultancy.

Pay / Benefits

  • competitive salary
  • health insurance
  • pension
  • on-site gym
  • hybrid working
  • career progression and training

Responsibilities

  • Lead and oversee qualitative, quantitative and mixed-methods research projects focused on PROs and COAs
  • Oversee selection, development, psychometric validation and implementation of COA measures
  • Own project delivery including timelines, contracts and financial performance
  • Act as primary client contact, steering COA strategy discussions with pharmaceutical teams
  • Design and supervise qualitative research and analysis alongside quantitative activities
  • Support regulatory interactions with agencies such as FDA and EMA
  • Critically review scientific and client-facing deliverables for quality and alignment
  • Lead project teams, allocate work and ensure timely delivery
  • Coach and mentor junior researchers and support their development
  • Build and maintain client relationships and identify follow-on opportunities
  • Contribute to proposals, project planning and wider business development
  • Support conference presentations, posters and journal publications

Key requirements

  • Extensive experience designing and conducting qualitative research with analysis and reporting
  • Experience developing and validating PRO measures or other COAs; understanding psychometric validation techniques
  • Experience supporting regulatory interactions with FDA, EMA or similar bodies
  • Strong project management skills with accountability for contractual and financial aspects
  • Experience leading research teams and supervising junior staff
  • Commercial awareness with client relationship development and follow-on work
  • Excellent written communication, presentation and stakeholder management
  • Knowledge of Good Clinical Practice, research ethics and data protection requirements
  • Experience in patient preference research or discrete choice experiments would be advantageous
  • Proven ability to work independently in a fast-paced consultancy environment
  • stakeholder management
  • leadership and mentoring
  • attention to detail
  • PROs and COA development and validation
  • qualitative and quantitative research methods
  • psychometric validation techniques

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Posted: October 16th, 2026