Generation of non-clinical and clinical documents (study reports, study protocols, investigator’s brochures, biomarker reports) and manuscripts for scientific publications
Quality control of documents
Close cooperation with other medical writers, statisticians, and project managers both within the company and on the client’s side
Organization/planning of trial team meetings
Your profile:
Education to an advanced degree level in a life science, medicine, or veterinary medicine discipline
At least 3 years of professional experience as a medical writer in clinical research
Knowledge in statistical evaluation of research results
Thorough understanding of ICH, GCP, and other relevant guidelines and regulations
Experience in literature research
Excellent editorial and proofreading skills
Ability to work in a team and a high degree of initiative
Communication skills with fluency in the English and German language both
