Medical Monitor (m/w/d)
2023-06-02
Full Time
Description
As a Medical Monitor, you will be closely involved in clinical studies by providing medical and scientific support for international and multi-centric clinical studies. Your main responsibilities:
- You serve as a point of contact for the study team, study sites and sponsors regarding the medical aspects of drug and medical device studies
- Review and conduct plausibility checks of medical study data and medical review of laboratory data and adverse event listings
- Monitoring of the safety aspects of clinical studies
- Evaluate adverse events/serious adverse events
- Support in the conception of clinical study designs and the development of study protocols.
- Review of clinical study reports and other study-specific documents
- Conduction of medical training for study teams (e.g. indication training)
- Participation in investigator meetings, study-specific monitoring boards and sponsor meetings
- Independently acquiring specialized medical knowledge (e.g. in specific indications).
- You have a medical licensure as a physician, preferably with a specialization in dermatology
- Experience in conducting clinical studies, ideally in dermatology
- Knowledge about patient care (hospital or practice) is desirable
- Interest in addressing scientific questions in the context of clinical studies
- Knowledge of ICH GCP, pharmaceutical laws and applicable national and international guidelines
- Strong organizational skills and ability to work in international project teams
- Self-motivated and goal-oriented
- Excellent written and verbal communication skills in German and English
- Advanced skills in using MS Office programs
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Hands-on mentality from the beginning - Flat hierarchies, open feedback culture and great team spirit
- Start-up meets grown-up mentality
- Exciting insights into clinical research
- Numerous benefits in addition to your salary