Clinical scientist (100%)

LimmaTech Biologics AG is a Swiss clinical stage biopharmaceutical company. We are advancing our proprietary vaccine pipeline to halt the increasing threat of global infections due to emerging antimicrobial resistance (AMR) and sexually transmitted diseases. Working at LimmaTech is a unique chance to be part of the development of life saving vaccines.

To support our Clinical team, we are currently looking for a:

Clinical Scientist (100%)

The Clinical Scientist contributes to the scientific and regulatory aspects of Phase I/II clinical trials, including trial design, clinical development plans, protocol development, statistical analysis plans, and clinical study reports, while reporting to the Associate Director Clinical Science. This is a 100% office-based role in Schlieren, with the possibility of one or two days of remote work per week.

You hold a Master’s or PhD in Life Sciences or a related field and have at least three years of experience in Clinical Development, with strong scientific and analytical skills. Demonstrated working experience in an industrial, biomedical research setting would be ideal.

As a Clinical Scientist, your responsibilities will include:

• Leading and managing the scientific aspects of Phase I and II clinical trials, ensuring adherence to scope, quality, budget, and timelines
• Designing and supporting clinical trials, clinical development plans, and regulatory strategies
• Preparing, reviewing, and maintaining clinical study documents, including protocols, study plans, and reports
• Analyzing, interpreting, and presenting clinical data internally and externally
• Identifying, coordinating, and developing clinical assays with external partners and clinical sites
• Conducting data checks, generating queries, and ensuring database integrity
• Managing and overseeing ethical and regulatory submissions, including clinical database registrations
• Selecting, managing, and overseeing external vendors such as CROs, clinical sites, and laboratories
• Authoring, revising, and updating SOPs, work instructions, and additional relevant documents
• Planning and conducting investigator meetings, training sessions, and key opinion leader meetings
• Coordinating and tracking clinical trial samples, investigational material, and other trial-related shipments
• Tracking and managing operational aspects of projects, including budgeting, risk management, and compliance with ICH-GCP and company SOPs

You are an efficient and enthusiastic team player with:

• Experience in regulatory affairs and submissions to agencies such as the FDA and EMA
• A solid background in statistics, with a focus on clinical trials
• Hands-on experience in managing operational aspects of clinical trials and developing all study-related documents
• Excellent planning and communication skills
• In-depth knowledge of ICH-GCP and experience in risk assessment and mitigation plan development
• The ability to thrive in a biotechnology environment with an entrepreneurial, fast-paced culture, where science-driven outcomes matter
• Strong verbal and written communication skills in English
• Proficiency in Microsoft Office 365 tools

We offer a friendly, highly motivated, and dynamic work environment located in Schlieren, near Zürich. The location is easily accessible by public transportation.

If you meet the requirements of this exciting position and want to contribute to our mission, we would love to hear from you. Please submit your detailed application, including a motivation letter, CV, diplomas and reference letters as one PDF file. Incomplete applications will not be considered. Please apply directly via our website, choose the vacancy on the right-hand side and fill in the application form. Please press the “Submit” button to send your detailed application.

Please note that due to visa regulations, only applicants eligible to work in Switzerland can be considered for this position.