Updated on 3 August 2026
eConsent Tool for Non-Interventional Studies
Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics
Düsseldorf, Germany
About
The eConsent functionality enables study participants to review and electronically sign the informed consent within the eCRF environment. It provides a secure digital workflow, enhances the participant experience, streamlines site operations, and supports regulatory compliance throughout the informed consent process.
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Medical Writing for Clinical Trials and Publications
Dr. Lucas-Sebastian Spitzhorn
Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics
Düsseldorf, Germany
Service
eCRF / EDC System for Clinical Research: Data and Trial Management
Dr. Lucas-Sebastian Spitzhorn
Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics
Düsseldorf, Germany
Service
- E-HEALTH
- MEDICINE
- Technology Transfer
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