Senior Director, Composite Measures & Integration

IQVIA; Paris; Sur place; EUR 180 000 - 230 000; Plein temps

Résumé du poste

IQVIA is seeking a Senior Director for Composite Measures Science & Integration to lead the design, development, validation, and deployment of scientifically rigorous composite measures in partnership with IQVIA Labs and external partners.

The role drives strategic, clinical, and regulatory development for laboratory- and genomic-enabled endpoints used in trials and real‑world settings, aligning with market needs and IQVIA solutions.

Qualifications

• Bachelor’s degree in a relevant scientific discipline; advanced degree preferred.
• At least 15 years of relevant scientific, drug‑development, or laboratory leadership experience.
• Deep knowledge of measurement theory, drug development, and instrumentation.
• Proven ability to influence across organizational boundaries and lead multiple workstreams.
• Strong communication, presentation, and client‑management skills.
• Ability to translate scientific insight into practical, scalable solutions.

Responsabilités

• Direct end‑to‑end development and delivery of composite measures integrating lab, genomic, and patient data.
• Ensure COA data collection and lab data meet scientific, privacy, and regulatory requirements.
• Lead research design, validation protocols, analytical methods, and technical reports.
• Oversee evaluation of laboratory measurement instruments in collaboration with IQVIA Labs.
• Provide leadership for cross‑functional initiatives with clients, regulators, and partners.

Connaissances

Leadership

Measurement theory

Strategic thinking

Communication

Client management

Formation

Bachelor’s degree in a relevant scientific discipline

Advanced degree preferred

Description du poste

IQVIA is seeking a Senior Director for Composite Measures Science & Integration to lead the design, development, validation, and deployment of scientifically rigorous composite measures in partnership with IQVIA Labs and external partners.

The role drives strategic, clinical, and regulatory development for laboratory- and genomic-enabled endpoints used in trials and real‑world settings, aligning with market needs and IQVIA solutions.