Research Scientist (Clinical Pharmacology)

TL;DR

Research Scientist (Clinical Pharmacology): Supporting bioanalytical and safety studies using ELISA and LC-MS/MS methodologies within a regulated laboratory environment with an accent on sample preparation, data integrity, and regulatory compliance. Focus on executing routine assay procedures, maintaining analytical equipment, and ensuring adherence to GCP/GCLP standards.

Location: Onsite in Merthyr Tydfil, United Kingdom

Company

hirify.global is a full-service CRO delivering clinical development solutions from first-in-man through Phase III for small and mid-size drug developers.

What you will do

• Process clinical study samples for routine assay procedures following Protocols, SOPs, and Work Instructions.
• Support Senior and Principal Scientists in sample analysis and method verification/validation activities.
• Manage general laboratory operations, including sample management, solvent logs, and waste disposal.
• Perform routine maintenance and calibration of laboratory instrumentation and equipment.
• Prepare and archive technical documentation, including protocols, validation reports, and SOPs.
• Ensure all activities adhere to good practice regulations and guidelines (GCP, EMA, and FDA).

Requirements

• BSc in a relevant scientific discipline or equivalent laboratory experience.
• Experience working within a laboratory environment, preferably supporting bioanalytical or safety studies.
• Proven ability to follow protocols and written instructions with high accuracy.
• Proficiency in Microsoft Office (especially Excel) for data documenting and reporting.
• Strong attention to detail and the ability to work effectively within a team under tight deadlines.
• Must be based in or able to work onsite in Merthyr Tydfil, UK.

Nice to have

• Degree in Analytical Science, Chemistry, Biochemistry, or Biomedical Science.
• Experience working in MHRA GCP, GLP, or GMP regulated environments.
• Hands-on experience with ELISA and/or LC-MS/MS analytical techniques.
• Familiarity with LIMS or other laboratory data management systems.
• Experience performing quality control activities and supporting laboratory compliance.

Culture & Benefits

• Permanent full-time employment.
• Work in a responsive and agile CRO environment.
• Opportunity to contribute to advancing medicine and improving patients' lives.
• Collaborative professional environment working alongside expert Senior and Principal Scientists.