Medical Monitor Clinical Development

Bioversys AG is an innovative biotech company in clinical-stage development in Basel. We are seeking a Medical Monitor to support global late-stage clinical trials in infectious diseases and antimicrobial resistance. The position reports to the Medical Director and plays a central role in overseeing complex, multi-regional studies — including Phase III trials across CIS countries, LATAM, China, the USA, and MEA.

This is an opportunity for a hands-on physician (MD) or a clinically experienced clinical research professional (CRO background welcome) who thrives in a dynamic, science-driven environment and is motivated to make a direct impact in the fight against antibiotic resistance.

Key Responsibilities

• Provide medical oversight for ongoing and upcoming clinical studies, ensuring patient safety and scientific integrity.
• Act as the medical liaison between investigational sites, CROs, and internal teams.
• Participate in study design, protocol review, and medical input to key clinical documents (IBs, CRFs, SAPs, CSRs).
• Be present at study sites as needed to support investigator engagement and study conduct (moderate travel).
• Contribute to safety review processes, including assessment of AEs/SAEs in collaboration with pharmacovigilance.
• Participate in data review meetings and contribute to IND and regulatory submissions.
• Support training and communication with site staff and internal stakeholders.
• Help shape and improve operational excellence in a growing clinical organization.

Qualifications & Experience

• Medical degree (MD or equivalent) strongly preferred; specialty in anesthesiology, internal medicine, or pneumology advantageous.
• Clinical experience with ICU or severely ill / chronic patients is highly desirable.
• 3–6 years of experience in clinical development, clinical operations, or medical monitoring within biotech, pharma, or CRO.
• Experience working on global trials and in multicultural settings outside the EU.
• Knowledge of infectious diseases or antibacterial drug development is an asset.
• Strong understanding of GCP, trial conduct, and regulatory standards (IND, CTA).
• Fluent in English; additional languages are an advantage.
• Proactive, curious, and adaptable personality, eager to work hands-on in a small, fast-evolving biotech team.

Why Join
This is a unique opportunity to work in an emerging, mission-driven biotech tackling antimicrobial resistance with novel therapeutics. You’ll collaborate closely with a small, passionate clinical team in Basel, gain broad exposure across global Phase II–III programs, and actively contribute to bringing life-saving medicines to patients worldwide.