Senior Regulatory Medical Writer - work from home, Europe
- Experience Level
- Experienced (non-manager)
I am helping one of my clients, one of the largest CRO's, find new team members for their Medical Writing teams. Looking to speak both to Medical Writers and Senior Medical Writers.
The company is growing rapidly, yet offering very stable and secure job opportunities. The team is lovely and you will really feel like part of a family. They work a lot with Oncology, so if it is your area of interest - you will get an insanely good experience.
The Senior Medical Writer, under the supervision of the Head of Medical Affairs Unit, is responsible for
drafting, editing and reviewing preclinical/clinical documents such as preclinical and clinical study reports,
study protocols, patient information and informed consent forms, and other medical and regulatory
documents (including Investigators' Brochure, IMPD, Briefing Document for Scientific Advice and follow-up
scientific advice, CTD).
Develops abstracts and scientific manuscripts reporting clinical trial results, as well as slide and poster
presentations, always working in compliance with regulations, Good Clinical Practices, ICH guidelines and
company standard operating procedures. Takes ownership of a given assignment, proactively collaborating
with Biometrics staff, Pharmacovigilance and Clinical Operations Units.
This role can be fully remote (Europe) - confirm specific countries with me.
- Master's degree in biomedical/scientific disciplines;
- At least 4 years of experience as a medical writer;
- Knowledge of medical concepts and terminology;
To find out more, please send your resume to email@example.com and I will get in touch.