Expert Scientific Writer

Expert Scientific Writer

8-18 years
Not Specified

Job Description

1. Demonstrate a command of assigned therapeutic areas and expertise with assigned products.
2. Research and write original content for publications activities (primary and review manuscripts, abstracts, posters), slide presentations and other materials based on direction and materials supplied by customers.
3. Prepare meeting materials for satellite symposia (agenda, slide content, speaker briefings etc), and reports from advisory boards and other internal or external meetings.
4. Develop content that is scientifically accurate, evidence-based, grammatically accurate, referenced using appropriate sources, and consistent with quality standards for author review, customer review as appropriate, and scientific peer review.
5. As needed, perform quality control (QC) checking / proof reading of the above mentioned documents to meet customer expectations.
6. Clearly communicate medical scientific concepts in a condensed, audience-appropriate way
7. Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP3.
8. Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed and to work on projects across multiple brands at any given time.
9. Interpret and apply clinical data in medical communication deliverables.
10. Work in conjunction with service team and line manager to develop and adhere to logical and attainable timelines for project completion.
11. Provide input and aid in troubleshooting/problem-solving.
12. Collate and incorporate author/customers comments.
13. Lead and/or participate in author/client teleconferences.
14. Provide accurate citations in text (utilizing Reference Manager system), a bibliography, and appropriately annotated references for medical review.
15. Participate in strategic and tactical publications planning and related research.
16. Work as part of a team; train new colleagues as and when required.
17. Supports people and performance management.
18. Maintains records for all assigned projects including archiving.
19. Maintains audit, SOP and training compliance.
20. Performs additional tasks as assigned.


Why Novartis

799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives

We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.

We are Novartis. Join us and help us reimagine medicine.

Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons.

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