350835BR
Aug 17, 2022
Poland

Job Description

Almost 1 billion! That’s how many lives our product touches globally.

Your Key Responsibilities:
Your responsibilities include, but not limited to:

•Translation and adaptation to polish language Products Text Information for newly registered products (SmpC/PIL/ labeling)
•Implementation of safety updates into Products Text Information based on Core Data Sheets
•Translation to polish and adaptation Risk Managements Plans and related educational materials
•Management and oversight of RA and medical part in RMP process, as well as readability tests preparation and management
• Dealing with medical inquiries related to products composition, pharmacology and toxicology etc
•Maintenance updated relevant set of procedures applying to Product Texts Management and RMP process
•SIL (shortened product information required in promotional materials) preparation for promoted products and maintenance up to date SIL database
•Co-leading management and oversight for internal system servicing medical inquiries

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

Minimum Requirements

What you’ll bring to the role:
Degree and a higher degree in life science; preferred medical or pharmaceutical faculty
Proficient use English language (ideally proved by language certificate )
•Scientific writing competency
•Proofreading and copyediting skills
•Strong knowledge and application of good practices in medical writing and regulatory requirements
•Experience with evaluating and reviewing medical / clinical/ regulatory content
•Ability to successfully manage assignments on time with high quality
•Good organization of work and tracking skills
•Willingness to undertake continuous professional learning and development
•Willingness to work in a matrix environment and to value the importance of teamwork
•Previous Scientific writing work experience is preferred but not essential

Why Sandoz?
500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we’re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world.

How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!

Imagine what you could do here at Sandoz!


Join our Novartis Group Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
NIBR
COMMERCIAL OPS EUROPE SZ
Poland
Warsaw
Human Resources
Full Time
Regular
No
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350835BR

Scientific Information Manager

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