Medical Monitor

vor 2 Wochen

Basel, Basel-Stadt, Schweiz gloor&lang AG Vollzeit CHF 80'000 - CHF 120'000 pro Jahr

About the Company

Our client is a dynamic European biotech company dedicated to the development of novel anti-infective therapies addressing antimicrobial resistance. Following successful clinical milestones and significant growth, the company is strengthening its clinical development team with an experienced and motivated Medical Monitor / Clinical Scientist.

About the Role

The Medical Monitor / Clinical Scientist will provide clinical and scientific oversight for ongoing and upcoming international studies in severe infectious diseases. The role combines operational, analytical, and medical-scientific responsibilities and offers broad exposure across clinical development.

This position is well suited for a PhD or PharmD with hands-on experience in clinical research who is ready to take on a central role in advancing innovative therapies within a fast-moving biotech environment.

Main Responsibilities

  • Provide clinical and scientific support for assigned clinical studies, ensuring compliance with study protocols, GCP, and regulatory requirements.
  • Act as primary contact for CRO medical monitoring teams and support investigator sites on protocol-related questions.
  • Review clinical data and safety listings; participate in data review and medical review meetings.
  • Contribute to the design of study protocols, amendments, and key clinical documents (IB, CRF, SAP, CSR).
  • Collaborate with pharmacovigilance, regulatory affairs, and biostatistics to ensure medical and scientific consistency across studies.
  • Support regulatory submissions and scientific reporting.
  • Provide medical-scientific input to internal project discussions and cross-functional development planning.

Qualifications & Experience

  • Advanced scientific degree (PhD, PharmD, or equivalent) in life sciences, pharmacology, or related field.
  • 3–5 years of experience in clinical development, medical monitoring, or clinical science within biotech, pharma, or CRO.
  • Sound understanding of clinical trial methodology and GCP.
  • Experience in infectious diseases or anti-infective drug development is an advantage.
  • Skilled in reviewing and interpreting clinical data and safety information.
  • Strong communication and problem-solving skills, proactive and hands-on working style.
  • Fluent in English (written and spoken); additional languages are a plus.

Why This Role

This is an opportunity to contribute directly to the development of novel treatments for life-threatening infections within an agile and purpose-driven biotech setting. The position offers broad visibility, close collaboration with clinical and scientific experts, and the potential to grow into senior development responsibilities.

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