Job Description:
A Clinical Research Associate (CRA) in Zurich plays a crucial role in managing clinical trials to ensure they adhere to Good Clinical Practice (GCP), regulatory guidelines, and company protocols. Responsibilities include site selection, initiation, monitoring, and close-out of clinical studies. The CRA is responsible for ensuring data accuracy, verifying patient eligibility, and overseeing the timely collection of trial documents. In Zurich’s highly regulated pharmaceutical environment, the CRA also acts as a liaison between the sponsor and the investigator site, ensuring effective communication and compliance. Regular travel to trial sites across Switzerland may be required for monitoring visits. The CRA prepares visit reports, resolves data queries, and supports ethics submissions. The role demands strong knowledge of trial procedures, excellent documentation skills, and the ability to manage multiple studies. Integrity, attention to detail, and effective communication are essential.
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.
