Pharmidex is pleased to offer an opportunity for a Bioanalytical Scientist with strong regulatory study experience to join our Bioanalytical team. This role is suited to an experienced scientist who enjoys hands-on laboratory work and delivering bioanalytical data for GLP and GCP-regulated studies.

You will support the execution of regulated bioanalytical studies from method development through to reporting, working closely with internal teams and, where appropriate, external clients.

Key Responsibilities

• Perform LC-MS bioanalysis in support of GLP/GCP-regulated studies
• Conduct method development, validation, and sample analysis
• Execute regulated study work in accordance with SOPs and QA expectations
• Prepare and review analytical data for study reports
• Maintain accurate documentation and laboratory records
• Support client interactions, data interpretation, and study discussions (dependent on experience)

Essential Experience & Skills

• Degree in Chemistry or a closely related discipline
• ≥5 years’ experience in a bioanalytical laboratory environment
• Demonstrable experience supporting regulatory (GLP and/or GCP) studies
• Strong hands-on experience with:
• Sample preparation
• Liquid chromatography and mass spectrometry
• Large molecule and peptide bioanalysis
• Experience in oligonucleotide bioanalysis
• Strong communication skills and ability to work within multidisciplinary teams

Desirable Experience

• Experience acting as Study Director or Principal Investigator for bioanalytical studies
• Prior client-facing responsibilities
• Knowledge of ADMET and drug discovery workflows
• Experience working within a CRO environment
• Exposure to biotherapeutics

Why Join Pharmidex?

Joining Pharmidex means becoming part of a high-performing CRO supporting regulated and non-regulated programmes for global clients. We value quality, accountability, and scientific excellence.