Job Description:
A Clinical Laboratory Manager in Geneva oversees the operations of a diagnostic or research laboratory that supports clinical trials and patient testing. This role includes managing laboratory staff, maintaining accreditation standards, ensuring accurate test results, and implementing quality control programs. The manager coordinates workflow, budgets, training, and regulatory compliance while supporting clinical research initiatives. In Geneva’s clinical research landscape, the manager works with principal investigators, sponsors, and regulatory bodies to ensure the integrity and reliability of laboratory services. They are responsible for laboratory audits, equipment validation, and maintaining high ethical standards in handling patient data and specimens. Strong leadership, technical proficiency, and communication skills are required. Familiarity with ISO 15189 and GCP standards is preferred.
Job Requirement:
Demonstrated experience in laboratory research, scientific data analysis, and technical reporting.
Proficiency in using laboratory equipment, software tools for data interpretation, and bioinformatics platforms.
Familiarity with GMP, GLP, GCP, and other regulatory compliance standards applicable to clinical and laboratory environments.
Strong documentation and record-keeping skills in accordance with industry standards.
Ability to design, execute, and troubleshoot experiments and assays independently or in a team.
Excellent written and verbal communication skills for preparing research documentation and collaborating across departments.
Detail-oriented with strong analytical thinking, problem-solving, and organizational capabilities.
Adaptability to fast-paced, collaborative, and evolving research and clinical settings.
Understanding of ethical research practices and commitment to maintaining data integrity and confidentiality.
Previous experience with clinical trials, product development, or regulatory processes is considered an advantage.
Ability to work with cross-functional teams including R&D, Quality, Regulatory, and Manufacturing.
Good time management skills and ability to meet tight project deadlines.
Fluency in English is mandatory; knowledge of German or French is a plus for Swiss workplaces.
Willingness to undergo ongoing training and certification as required by the organization.
