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ServiceUpdated 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

  • Trial Design Outline (TDO) & Trial Protocol (CTP)

  • Investigators Brochure (IB)

  • Informed Consent (IC)

  • Clinical report form (CRF/eCRF)

During the trial

  • Amendment (e.g. changes to the protocol)

  • IB update

After trial conduct

  • Clinical trial report (CTR)

  • Biomarker Report

  • Publication

  • Slide deck generation

Quality control of documents

  • Completeness and consistency

  • Fulfilment of sponsors requirements

  • Formatting and layout

  • In-text tables/figures

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