Role Overview
My client is a CRO that supports pharmaceutical development from early preclinical phases through late-stage clinical research, supporting the development of the next generation of therapeutics.
The principal scientist will provide high-level scientific and technical leadership across bioanalytical activities, with a focus on LC/MS/MS method development, validation and project management for NCE, proteins, peptides, oligonucleotides and Drug Conjugates.
Key Responsibilities
* Lead and oversee bioanalytical method development projects, particularly for NCEs, small molecules, peptides, and oligonucleotides.
* Coordinate GLP/GCP-compliant method development and validation (ICH) for quantifying drugs, metabolites, and biomarkers in biological matrices using LC-MS/MS.
* Provide scientific direction, troubleshooting, and interpretation for complex and high priority client projects.
* Maintain transparent, client-oriented communication with clients, ensuring scientific proposal writing, project scoping, and technical discussions and timely updates.
* Support business development through generation of marketing material as well as presenting at key scientific conferences
Qualifications
* Extensive experience in Bioanalytical LC-MS/MS method development and validation.
* Strong experience with proteins, peptides is highly valued.
* Experience as a project leader coordinating and managing multiple projects simultaneously.
* Solid understanding of international bioanalytical guidelines;
experience working under GLP/GCP.
What Is Offered
* Salary up to €60,000 DOE
* Opportunity to contribute to the continued success and growth of an expanding, high-quality CRO.
* Strong career progression opportunities to a Management role outlined from day 1.
* Access to cutting-edge laboratory technology and modern analytical platforms.
* A professional, diligent organisation with a human touch, strong values, and a commitment to excellence.