Medical Monitor

Eurofins

Hamburg, HH, Germany Remote permanent

Posted: April 28, 2026

Quick Summary

Medical Monitor is responsible for ensuring the safety and efficacy of dermatological products through thorough monitoring of clinical trials, providing expert guidance to pharmaceutical companies to drive the development and launch of new treatments. The ideal candidate will have experience in a regulatory affairs or clinical trials setting, with strong communication and analytical skills. This role requires a unique blend of technical expertise in dermatology and regulatory compliance, as well as excellent project management skills.

Job Description

Eurofins bioskin is a leading niche CRO with unique understanding and capabilities for both early and late phase development of dermatological and related products. Since its inception in 1992, eurofins bioskin has been recognized as a valuable partner for dermatological product development. Starting as a small Contract Research Organization (CRO) specialized in conducting early phase safety and efficacy trials, eurofins bioskin has grown into a full-service CRO offering global dermatologic consulting and regulatory services and all services for management of Phase I-IV drug trials and claim support/safety studies. eurofins bioskin is headquartered in Hamburg, Germany.

The Medical Monitor is responsible for providing medical oversight during the conduct of clinical studies (ranging from single-center to multi-center, multinational studies) managed by bioskin, the goal being to ensure the safety and clinical integrity of participating subjects/patients.

Principal Responsibilities and Duties:

•       Ongoing review of laboratory and ECG alerts

•       Medical expertise and guidance for project team and clinical sites regarding subject/patient eligibility and safety issues and any protocol-related medical questions during study conduct

•       Safety review of AEs/SAEs

•       Review of medical data listings including vital signs, concomitant medication, medical history, laboratory data, amongst other data

•       Medical assessment of protocol deviations

•       Participates in project team meetings and medical team meetings and serves as medical interface between sponsors and clinical site teams.

Qualifications & Skills:

•       MD licensed in Germany, preferably with specialization in dermatology

•       Basic knowledge of clinical research and ICH-GCP required, previous experience 

         in  medical monitoring an additional asset

•       Very good English and German (both written and spoken)

•       Proactive working style, strong teamworking and communication skills

•       Analytical skills and close attention for detail

•       Working time 20 – 30 hours per week

Contacts by headhunters, recruiting or staffing agencies are not accepted!

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