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Consultant – Qualitative Patient-Centered Research

Consultant – Qualitative Patient-Centered Research

CompanyIQVIA
LocationPointe-Claire, QC, Canada
Salary$Not Provided – $Not Provided
TypeFull-Time
DegreesMaster’s, PhD
Experience LevelMid Level

Requirements

  • Master’s degree or PhD in a relevant field (or substantial experience with a Bachelor’s degree)
  • 3 years of relevant experience in a related field including Psychology, Epidemiology, Sociology, Economics, Statistics, Public Health, or other social science-related field
  • Experience conducting qualitative individual in-depth interviews (preferably concept elicitation and cognitive debriefing) and/or focus groups
  • Experience using qualitative software (such as NVivo or Atlas.ti)
  • Proven scientific track record
  • At least 5 abstracts accepted for presentation at a major scientific venue, or equivalent experience teaching college-level curriculum or industry workshops
  • At least 1 peer-reviewed published article or equivalent experience (such as large number of complex unpublished technical reports for clients, internal statistical manuals or documentation, etc.)
  • Knowledge of qualitative research design, data collection, and analysis of qualitative data
  • Knowledge of ICH GCP, 21 CFR Part 11 compliance or experience working in a highly regulated industry would be an asset
  • Ability to independently analyze qualitative data based on an analysis plan provided a senior team member is required
  • Strong written and verbal communication skills are required
  • Qualitative interview skills are required

Responsibilities

  • Conducts literature reviews and summarizes into scientific outputs
  • Supports and assists research teams with study design, development of study materials (i.e., protocols and interview guides), data management, and quality assurance
  • Conducts qualitative in-depth interviews; moderates focus groups
  • Analyzes and interprets data from interviews and focus groups
  • Co-authors technical reports, summaries, manuscripts, posters, and presentations
  • Prepares for and presents at professional meetings and client-sponsored events, and prepares and publishes associated abstracts
  • Proactively problem solves; identifies and helps drive resolution of issues at all phases of the project that could affect success
  • Manages projects efficiently and effectively within guidelines of company and department operating procedures
  • Reports on projects to supervisor or senior leadership as necessary
  • Interacts with clients, clinical experts, and research support staff to ensure that projects are completed in a timeline fashion and in accordance with quality standards and Standard Operating Procedures
  • Interacts effectively and collegially with all employees, fostering a supportive and cross departmental sharing environment

Preferred Qualifications

  • Knowledge of ICH GCP, 21 CFR Part 11 compliance or experience working in a highly regulated industry would be an asset