Bioanalytical Scientist (Regulatory Studies)

Pharmidex; Hatfield; On-site; GBP 40,000 - GBP 60,000; Full time

Job summary

A leading contract research organization in the UK seeks an experienced Bioanalytical Scientist to support GLP and GCP-regulated studies. The ideal candidate will have over 5 years' experience in a bioanalytical lab, with strong skills in LC-MS bioanalysis and regulatory study support. This role involves hands-on work in a collaborative environment, preparing reports and maintaining documentation. Applicants should demonstrate strong communication skills and client-facing experience. Interested candidates should apply via email.

Qualifications

• 5+ years of experience in a bioanalytical laboratory.
• Experience supporting GLP and/or GCP studies.
• Experience acting as Study Director or Principal Investigator.

Responsibilities

• Perform LC-MS bioanalysis for regulatory studies.
• Conduct method development, validation, and sample analysis.
• Prepare and review analytical data for study reports.

Skills

LC-MS bioanalysis

Liquid chromatography

Mass spectrometry

Oligonucleotide bioanalysis

Communication skills

Client-facing experience

Education

Degree in Chemistry or related discipline

Job description

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:
• Liquid chromatography and mass spectrometry
• Large molecule and peptide bioanalysis
• Experience in oligonucleotide bioanalysis
• Strong communication skills and ability to work within multidisciplinary teams
• 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.

Apply

Please send your CV and a short cover note to [e-mail]