- As a member of the Global Digital Hub Team, you will play a crucial role in advancing the long-term outcomes and strategy of the Global Digital Hub, while also prioritizing the delivery of high-quality content.
- In your capacity as a medical writer, you will focus on crafting medical writing and digital content solutions and focus on upholding the highest standards of scientific accuracy, quality and compliance.
- You will also be responsible for maintaining a strong knowledge of medical terminology, guidelines, and regulations to ensure the accuracy and quality of all content produced.
- To dive deeper, you will take the lead in developing an end-to-end content creation process and overseeing its successful delivery. In addition, you must stay up to date on industry trends and best practices in medical writing and content creation.
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
