Principal, Regulatory Strategy & RWE Solutions

IQVIA; Illkirch-Graffenstaden; Sur place; EUR 120 000 - 150 000; Plein temps

Résumé du poste

IQVIA in Illkirch-Graffenstaden, France, is seeking a Principal (Director-level) to own delivery leadership for Regulatory Science and Strategy, lead standalone regulatory strategy engagements, and drive cross-functional RWE studies for regulatory decision-making across drugs, biologics and devices.

The role requires senior client engagement, proposal development, EMA/FDA knowledge, and a track record of leading teams, shaping strategic directions, and delivering high-quality insights to clients

Qualifications

• Strong academic background in life sciences or related field with regulatory focus.
• Experience in regulatory science, regulatory strategy, or product review.
• Proven ability to lead client engagements and multiple workstreams.
• Willingness to travel to client locations and operate in a consulting setting.
• Fluency in English (spoken and written).

Responsabilités

• Lead selling and delivery of standalone RSS regulatory strategy engagements end-to-end.
• Collaborate with IQVIA Real World Solutions teams on RWE generation programs.
• Develop regulatory strategy proposals and support cross-functional delivery.
• Mentor junior consultants and contribute to RSS capability building.
• Maintain awareness of EMA guidance and harmonization globally.

Connaissances

Industry and regulatory expertise

Real world data expertise

Regulated medical product experience

Client relationship management

Business development

Solution selling

Communication and executive presence

Cooperative teamwork

People leadership / mentoring

Strategic thinking

Formation

Graduate degree preferred (PharmD/PhD/MD/MPH/MS)

Description du poste

IQVIA in Illkirch-Graffenstaden, France, is seeking a Principal (Director-level) to own delivery leadership for Regulatory Science and Strategy, lead standalone regulatory strategy engagements, and drive cross-functional RWE studies for regulatory decision-making across drugs, biologics and devices.

The role requires senior client engagement, proposal development, EMA/FDA knowledge, and a track record of leading teams, shaping strategic directions, and delivering high-quality insights to clients