Medical Monitor - Global Clinical Development

Bioversys AG is an innovative biotech company in clinical-stage development in Basel. To grow the team, 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 ResponsibilitiesProvide 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 & ExperienceMedical 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 JoinThis 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.