Job Description:
The Biomedical Research Associate in Geneva contributes to translational research projects involving disease mechanisms, diagnostics, and drug development. The role entails conducting laboratory experiments involving animal models, cell lines, and tissue cultures. Associates are responsible for generating, analyzing, and interpreting biological data using statistical and visualization software. Collaborating with academic and clinical teams, the associate supports publications, grant submissions, and regulatory documentation. In Geneva, this role may also involve contributing to global research initiatives or working with WHO-affiliated projects. It demands meticulous attention to scientific protocols, laboratory safety, and ethical research guidelines. Strong teamwork and clear communication are necessary for success.
Job Requirement:
Bachelor’s, Master’s, or Ph.D. in Biotechnology, Molecular Biology, Life Sciences, Biochemistry, or a related field.
Strong understanding of biological systems, scientific methodologies, and lab safety protocols.
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.
