Description
We are looking for our client, an international renowned biopharmaceutical company, for a
Medical Writer (m/f)
Reference: -en
Start: asap
Duration: 36 MM
Place: in the Basel region
Branch: Herstellung von pharmazeutischen Erzeugnissen
Your tasks:
- Act as a Transparency Specialist to comply with the clinical report publication requirements under EMA Policies and the Clinical Trial Regulation
- Writing clinical study reports and other documents as required
- Supporting and contributing to educational activities
- Overseeing evolving regulatory requirements and serving as a contact point and expert
- Identifying potential tools and managing external vendors providing specialized anonymization services
- Creating and maintaining Standard Operating Procedures and Working Instructions
Your qualifications
- Experienced Medical Writer with demonstrated Life Sciences industry background
- Bachelor degree in Life Sciences or equivalent educational background with the combination of the required skills
- Experienced in clinical report publication requirements under EMA policies and the Clinical Trial Regulation
- Proficiency in the writing of clinical study reports
- Profound user skills regarding MS Office
- Excellent, up to native-level English language skills, in both verbal and written form
Skills:
- Regulatory affairs assistant
- Medical affairs manager
- Medical writer
Keywords: Medical Affairs Manager