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).
Your qualifications:
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
We offer great opportunities!
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
Are you interested? Apply now! We look forward to receiving your application, including your salary expectations and earliest possible start date.
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