Medical Writer

Your (day to day) responsibilities will include, but are not limited to :

• Writing and editing CTDs, CSRs, IBs, protocols, manuscripts, and summaries, amongst other documents required for regulatory submissions
• Ensuring that the content, format, and structure comply with regulatory and other guidelines, as we'll as with Roches best practices
• Proactively contributing with creative ideas, concepts, or suggestions to provide added value
• Working cross-functionally with global teams and pharma affiliates to develop various project deliverables
• Partnering with the creative design team to develop infographics, images, etc
• Diligently keeping up to date with and following all applicable company standard operating procedures (SOPs) to meet quality standards
• Performing quality checks and proof-reading for accuracy

Who you are

• You hold a bachelors degree in medical sciences or equivalent eg MBBS, Dentistry, PhD in Healthcare, Pharmacology and 5+ years of experience in a similar role. Preferably, a relevant certificate in medical writing, regulatory affairs, etc
• The ability to interpret medical and clinical dats

Skills Required

Clinical Research, Medical Terminology, Data Analysis, literature review