Research Scientist (ELISA/LC-MS/MS)

Location: Merthyr Tydfil, United Kingdom

Company

hirify.global is a full-service contract research organisation delivering clinical development studies from first-in-human through Phase III for small and mid-size drug developers.

What you will do

• Process clinical study samples, including sample preparation, extraction, and preparation of chemicals, reagents, and solutions.
• Perform and support bioanalytical and safety study analyses using ELISA and LC-MS/MS methodologies.
• Assist with method verification and validation activities under the guidance of Senior and Principal Scientists.
• Maintain laboratory operations, including sample management, consumable and reagent control, solvent logs, databases, waste management, and laboratory readiness.
• Perform or support routine maintenance and calibration of laboratory instruments and equipment.
• Prepare and maintain protocols, procedures, validation and study reports, SOPs, CAPAs, file notes, and other study documentation.

Requirements

• BSc in a relevant scientific discipline or equivalent laboratory experience.
• Experience working in a laboratory environment, preferably supporting bioanalytical or safety studies.
• Ability to follow protocols, SOPs, and written instructions accurately.
• Experience using standard laboratory equipment such as pipettes, centrifuges, and balances.
• Proficiency in Microsoft Office, particularly Excel, for documenting, analysing, and reporting data.
• Strong organisational, communication, documentation, accuracy, and teamwork skills.

Nice to have

• Degree in Analytical Science, Chemistry, Biochemistry, Biomedical Science, or a related discipline.
• Experience in regulated environments such as MHRA GCP for laboratories, GLP, or GMP.
• Experience with ELISA, LC-MS/MS, HPLC, LIMS, sample extraction, bioanalytical workflows, or laboratory compliance activities.
• Experience documenting analytical activities and preparing reports to GxP standards.

Culture & Benefits

• Work in a regulated laboratory environment focused on accuracy, data integrity, quality, and compliance.
• Collaborate with Senior Scientists, Principal Scientists, Laboratory Project Managers, and wider laboratory teams.
• Contribute to clinical development studies intended to improve patient outcomes.
• Operate within a responsive and agile CRO providing tailored and scalable solutions to clients.