Laboratory Technician. Clinical Biomarkers

Job Description

We are looking for a Laboratory Technician to join the Clinical Biomarkers team within the Drug Development Department.

The successful candidate will join a team working on different clinical development projects and will be involved in both the execution of laboratory analyses and the organization and management of laboratory activities.

We are looking for an experienced and independent person, able to organize and plan their work, follow up on laboratory activities, and support the area manager with technical and organizational tasks.

 

Main Responsibilities

  • Perform biomarker assays, mainly using molecular biology techniques and immunoassays.
  • Prepare samples, reagents, materials, and equipment required for analyses.
  • Organize and plan laboratory activities according to project needs and timelines.
  • Manage inventory, reagents, materials, and storage conditions.
  • Monitor the status and maintenance of laboratory equipment, including calibrations and routine checks.
  • Record and track samples, results, and study-related documentation.
  • Participate in the development, optimization, and validation of new assays for the analysis of clinical samples.
  • Perform preliminary analysis of results and provide support in resolving technical issues.
  • Collaborate with CROs, suppliers, external laboratories, and other teams when required.
  • Support the area manager with planning and follow-up of activities, documentation, and other laboratory organizational tasks.
  • Propose and implement improvements to laboratory processes and organization.

 

Requirements

  • Technical laboratory qualification (CFGS) or a degree in Biology, Biotechnology, Biochemistry, Biomedical Sciences, or a related field.
  • At least 3 years of laboratory experience, preferably in biomarkers, molecular biology, drug development, or clinical sample analysis.
  • Practical experience with molecular biology techniques and/or immunoassays.
  • Experience working under quality systems (ISO, GLP, or similar).
  • Ability to work independently and organize different tasks and priorities.
  • High level of written English, to work with protocols, procedures, reports, and scientific and technical documentation.
  • Good knowledge of Microsoft Office, especially Excel, Word, and PowerPoint.

 

Desirable Qualifications

  • Experience working with samples from clinical trials.
  • Experience in immunoassay development and validation.
  • Experience with proteomics techniques (ELISA, Western Blot, immunofluorescence) and/or genomics techniques (qPCR).
  • Experience in the management and traceability of biological samples.
  • Experience coordinating with CROs, suppliers, or external laboratories.
  • Experience organizing and planning laboratory activities.
  • Knowledge of GraphPad Prism or other data analysis tools.
  • Good level of spoken English.

 

Profile

We are looking for an organized, rigorous, and practical person who can work independently and anticipate the needs of the laboratory.

We particularly value initiative, problem-solving skills, and an interest in progressively taking on additional responsibilities within the team.