Head of Pharmacokinetics

RBW Consulting; Lille; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

A clinical stage biotech company in Lille is seeking a Head of Pharmacokinetics to lead DMPK and ADME-Tox strategies across preclinical and clinical development. This role involves designing Phase I clinical trials, managing CRO/vendor relationships, and ensuring scientific excellence. The ideal candidate holds a Ph.D. in pharmacokinetics and has at least 5 years of experience in a pharmaceutical environment, alongside proven leadership and strong regulatory knowledge. Collaboration with cross-functional teams is essential.

Qualifications

• 5 years’ experience in a pharmaceutical company or CRO.
• Strong knowledge of clinical trial regulations, GLP / GCP, and ICH guidelines.
• Proven leadership and communication skills.

Responsabilités

• Lead and coordinate DMPK and ADME-Tox studies for development projects.
• Design Phase I clinical trials and contribute to other study designs.
• Oversee CRO / vendor selection and ensure quality delivery.

Connaissances

Leadership

Project management

Pharmacokinetics expertise

Regulatory knowledge

Fluent in English

Formation

Ph.D. specialized training in pharmacokinetics

Description du poste

Are you an expert in pharmacokinetics with a passion for driving innovation in drug development? RBW are partnered with a clinical stage biotech as they're looking for a Head of Pharmacokinetics to lead and shape their DMPK and ADME-Tox strategies across preclinical and clinical development. This is a unique opportunity to lead a critical function in drug development, influence strategy, and work on innovative projects that make a real impact. You’ll collaborate with cross-functional teams and contribute to shaping the future of the pipeline.

This will be responsible oversee all pharmacokinetic activities, including bioanalysis, PK / PD, population PK, and PBPK modelling, while ensuring scientific excellence and regulatory compliance. You’ll manage external vendors, contribute to project strategies, and play a key role in designing Phase I trials and non-clinical studies.

Key Responsibilities

• Lead and coordinate DMPK and ADME-Tox studies for development projects.
• Design Phase I clinical trials and contribute to other study designs.
• Oversee CRO / vendor selection and ensure quality delivery.
• Drive modelling activities (popPK and PBPK).
• Provide scientific input for regulatory documents and publications.
• Build and maintain a network of experts and foster innovation within the team.

Requirements

• Ph.D specialized training in pharmacokinetics.
• 5 years’ experience in a pharmaceutical company or CRO.
• Expertise in pharmacokinetics, metabolism, and modelling approaches.
• Strong knowledge of clinical trial regulations, GLP / GCP, and ICH guidelines.
• Proven leadership, project management, and communication skills.
• Fluent in English (written and spoken).