Beschreibung
Medical Writer (m/f)
Reference: -en
Start: asap
Duration: 8 MM+
Main tasks:
- Write and review clinical regulatory documents such as clinical study reports, investigator’s brochures and CTD Module II summaries
- Collaborate with Regulatory Project Managers, Clinical Science Leaders, and the International Project Team
- Assist in the preparation and review of clinical study protocols and statistical analysis plans
- Work together with the in-house Documentation Group to produce high-quality documents in compliance with regulatory requirements
- Manage external medical writing services
Main qualifications
- A degree in life sciences (BSc and/or MSc/PhD)
- English native level
- Well developed and proven medical writing skills
- Solid experience as a medical writer in the pharmaceutical industry across several therapeutic areas
- The ability to develop and mentor more junior medical writers
- Knowledge of regulatory document requirements and guidelines
- The ability to work independently and as part of a team
- The ability to work under pressure and meet challenging deadlines
- Excellent interpersonal and presentation skills
Main advantages:
- A city with a high quality of life that perfectly embraces both modern and traditional values
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Andrea Beck
Referencenumber:
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