(Senior) Medical / Scientific Writer*

at  Immatics Biotechnologies GmbH

ABOUT US

Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. Operating from Tuebingen, Munich and Houston, we are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer. For more detailed information, visit www.immatics.com.

• Editorial work in the publication process of preclinical and clinical studies and results, e.g. as abstracts, poster presentations or publications in peer-reviewed scientific journals. E.g., coordination of authoring process with scientific and non-scientific experts from various departments, refinement of written and visualized content, responsibility for the submission process.
• Preparation of regulatory documents required for clinical trial application submissions in Europe and IND submissions in the USA in order to obtain approval for the conduct of clinical trials investigating innovative cancer immunotherapies (e.g., clinical trial protocols and amendments, investigator’s brochures, Investigational Medicinal Product Dossiers)
• Preparation of briefing books required for scientific advice meetings in Europe and in the USA.
• Writing of medical and/ or scientific sections, planning and developing of document strategies, resolving review comments with the respective R&D colleagues, and oversight of timelines.
• Quality assurance/ control of documents, oversight of medical/ scientific writing projects assigned to external vendors.
• Research on scientific or clinical development topics based on scientific literature and integration of key results into regulatory documents or summaries for internal purposes