Head of Pharmacokinetics

RBW Consulting; Nice; Sur place; EUR 80 000 - 100 000; Plein temps

Résumé du poste

A clinical stage biotech company is seeking a Head of Pharmacokinetics to drive innovation in drug development. This leadership role involves overseeing pharmacokinetic activities, managing external vendors, and designing Phase I trials. Candidates should have a Ph.D. in pharmacokinetics, over 5 years’ experience in the pharma or CRO sector, and expertise in regulatory standards. Join us to shape the future of critical drug development projects in a collaborative environment.

Qualifications

• Minimum of 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.

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.
• 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.

Connaissances

Pharmacokinetics expertise

Project management

Communication skills

Formation

Ph.D. 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).