Pre-Clinical Project Leader

Noucor; Palau-solità i Plegamans; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A pharmaceutical company based in Palau-solità i Plegamans is seeking a Pre-Clinical Project Leader to coordinate drug development activities. This role involves leading non-clinical programs, including pharmacology and toxicology, and requires 2-5 years of experience in pre-clinical drug development. The ideal candidate will have a university degree in health sciences or pharmaceutical sciences and strong knowledge of ICH guidelines. We offer a competitive benefits package and a supportive work environment focused on well-being.

Servicios

Competitive benefits package

Flexible schedule

Wellness Plan (physiotherapy, online psychology services)

Formación

• 2-5 years of experience in pre-clinical drug development in pharma or biotech.
• Experience managing non-clinical studies.
• Strong knowledge of pharmacology, toxicology, and DMPK principles.

Responsabilidades

• Execute pre-clinical development strategies to support drugs under development.
• Lead non-clinical programs including pharmacology, toxicology, safety pharmacology, and DMPK.
• Contribute to regulatory submissions.

Conocimientos

Project management

Knowledge of ICH guidelines

Safety pharmacology

Excellent communication skills

Cross-functional teamwork

Advanced English (C1)

Educación

University education in health sciences or pharmaceutical sciences

Descripción del empleo

Do you want to be part of a team with a real impact on global health?

At Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide 🌍.

We are currently looking for a Pre-Clinical Project Leader to join Noucor’s Clinical and Preclinical Development Team.

The Pre-Clinical Project Leader leads and coordinates non-clinical development activities to support the progression of drug candidates from non-clinical phase to early clinical development. This role ensures that pharmacology, toxicology, DMPK, and all related non-clinical studies are scientifically sound, regulatory-compliant, and aligned with overall development strategy.

Responsabilities

• Execute pre-clinical development strategies in support of drugs under development.
• Lead non-clinical programs including pharmacology, toxicology, safety pharmacology, and DMPK.
• Support on the design, oversee, and review all in vivo and in vitro non-clinical studies conducted at CROs
• Participate in the selection and management of CROs.
• Review study protocols, study report and all study deliverables in alignment with internal SOPs and current legislation.
• Ensure studies are conducted in compliance with GLP and relevant regulatory guidelines
• Ensure that the studies are aligned with internal timelines and budgets.
• Contribute and prepare the non-clinical part of the regulatory submissions.

Requirements

• University education in health sciences, pharmaceutical sciences or related field.
• 2-5 years of experience in pre-clinical drug development in pharma or biotech
• Experience managing non-clinical studies
• Strong knowledge of non-clinical safety requirements (ICH M3, M12, S7, S9, etc.), pharmacology, toxicology, and DMPK principles.
• It will be valuable previous experience also in clinical phase development (phase I-IV)
• Excellent written and verbal communication
• Ability to work in cross-functional environments
• Advanced English (C1)

We Offer

⚙️ Work within a great team of professionals with a very good work environment.

🚀 Innovative work environment focused on continuous improvement.

❤️ Competitive benefits package and flexible schedule.

🧘🏻 ♀️ We care about your well-being – the Wellness Plan includes physiotherapy, online psychology services, sports events, and more.

📍 Offices in Palau-solità i Plegamans.

Interested in joining us?

At Noucor, we believe in the value of diverse teams. We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic.

If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you.