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IQVIA

Runs drug trials and sells health data to pharma

Head of Patient Science - Instrument Development & Thought Leadership

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeParis, FranceNo salary listedIn-person

About the Job

Requirements

  • An advanced degree (PhD, Master's, or equivalent) in Psychology, Behavioral Measurement, Health Services Research, Epidemiology, Pharmacy, Public Health, or a related discipline.
  • At least 10 years of professional experience in COA/outcomes research within pharmaceutical, CRO, or consultancy settings, with a strong track record of publications.
  • Deep understanding of COA methodology, psychometrics, FDA/EMA regulatory guidelines on patient-focused drug development, and qualitative research methods.
  • Excellent scientific writing and verbal communication skills, including the ability to communicate complex data to regulatory bodies and internal senior leadership.
  • Proven influencing skills at senior management level, with the presence and credibility to engage and influence senior leaders across multiple geographies and functions.
  • Demonstrated success building effective relationships with global stakeholders, including senior leaders, business and technical teams, go-to-market teams, and customers.
  • Proven experience managing high-performing teams, building talent, and influencing cross-functional stakeholders.
  • Promote information sharing, demonstrate flexibility in a fast-paced, dynamic environment, and effectively manage change.
  • Submit a CV in English.

Responsibilities

  • Define instrument development strategies across therapeutic areas, aligned with Instrument Licensing & Services, R&DS Therapeutic Area Priorities and goals, FDA/EMA guidance on patient-focused drug development, and health technology assessment requirements.
  • Lead development, validation, and implementation of new and existing clinical outcome assessment instruments, including psychometric evaluation, qualitative research, and endpoint definition.
  • Support the Scientific & Strategic Research Consulting team on client-facing clinical outcome assessment endpoint strategy projects as needed.
  • Lead regulatory interactions concerning newly developed clinical outcome assessments intended to replace older assessments that are declining in relevance.
  • Direct advanced methodologies, with emphasis on Domains of Health, including Digital Measurement Plans, electronic clinical outcome assessment strategies, and Patient Experience Data analytics.
  • Partner with Instrument Licensing & Services, Strategic & Scientific Research, R&DS Design & Delivery Innovation, therapeutic area centers of excellence, clinical operations, biometrics, regulatory, and commercial teams to build, expand, and enhance clinical outcome assessment utility in measuring meaningful health change.
  • Mentor and build a team of experienced and developing scientists, guiding them in clinical outcome assessment methodologies and scientific best practices.
  • Participate in acquisition science and staff integration related to clinical outcome assessment assets and scientific subject-matter experts.
  • Represent the company at scientific conferences and in industry consortia.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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