Medical Monitor (m/w/d)

SThree

Hamburg

On-site

EUR 70,000 - 90,000

Full time

14 days+

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Job summary

A leading healthcare staffing agency is seeking a Medical Monitor to ensure patient safety and protocol compliance in clinical trials focused on dermatology. The ideal candidate is a licensed physician with a strong background in medical monitoring and experience in dermatological research. This is a full-time, on-site position located in Hamburg, requiring fluency in both German and English.

Qualifications

  • Experience in dermatology (clinical or research).
  • Proven track record in medical monitoring within clinical trials.
  • Strong understanding of GCP and clinical development processes.

Responsibilities

  • Provide medical oversight for clinical trials, ensuring patient safety.
  • Review and assess clinical data, including adverse events.
  • Collaborate with cross-functional teams including clinical operations.

Skills

Medical monitoring
Fluent in German
Fluent in English

Education

German medical license (Approbation)

Job description

Overview

We are currently seeking an experienced Medical Monitor to support clinical development activities in the field of dermatology. This is a fully on-site position based in Hamburg, ideal for a licensed physician with hands-on experience in medical monitoring and a strong interest in dermatological research.

Location and Employment

Location: Hamburg, Germany
Employment Type: Full-time, permanent

Key Responsibilities
  • Provide medical oversight for clinical trials, ensuring patient safety and protocol compliance
  • Review and assess clinical data, including adverse events and medical narratives
  • Collaborate with cross-functional teams including clinical operations, safety, and regulatory affairs
  • Serve as medical point of contact for investigators and study teams
Requirements
  • German medical license (Approbation)
  • Experience in dermatology (clinical or research)
  • Proven track record in medical monitoring within clinical trials
  • Strong understanding of GCP and clinical development processes
  • Fluent in German and English
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