Medical Monitor (Clinical Development – Infectious Diseases) at gloor&lang AG

Basel, Basel-City, Switzerland -

Full Time

Start Date

Immediate

Expiry Date

13 Jan, 26

Salary

0.0

Posted On

15 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Medical Monitoring, Clinical Development, Infectious Diseases, Data Review, Safety Information, Study Protocols, GCP, Pharmacovigilance, Regulatory Affairs, Biostatistics, Problem-Solving, Communication, Analytical Skills, Collaboration, Proactive Working Style

Industry

Staffing and Recruiting

Description

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.

Responsibilities

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