Updated on 3 August 2026
Medical Writing for Clinical Trials and Publications
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
Prior to approval
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Trial Design Outline (TDO) & Trial Protocol (CTP)
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Investigators Brochure (IB)
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Informed Consent (IC)
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Clinical report form (CRF/eCRF)
During the trial
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Amendment (e.g. changes to the protocol)
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IB update
After trial conduct
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Clinical trial report (CTR)
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Biomarker Report
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Publication
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Slide deck generation
Quality control of documents
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Completeness and consistency
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Fulfilment of sponsors requirements
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Formatting and layout
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In-text tables/figures
Organisation
Similar opportunities
Service
Statistical Consultancy / Planning / Analysis for Clinical Trials
- Consulting
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
eConsent Tool for Non-Interventional Studies
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