Global Medical Writing Manager
Ipsen is a growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health and quality of life, providing effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology, Neurosciences, and Rare Diseases.
Why Ipsen?
- Patient‑Focused: The patient is at the heart of everything we do, and improving their outcomes is the deliverable of every strategy.
- Employee Care: We care for our employees, who are the ambassadors making a real difference.
- Bold Leadership: We attract and develop bold, agile, entrepreneurial individuals who take full ownership of their decisions.
- Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast‑moving, game‑changing organization.
About The Role
The Medical Writer Specialist is responsible for the generation of consistently high‑quality clinical documentation content and capable of working across multiple accounts and projects seamlessly, and is the scientific expert in their allocated therapy areas and can accurately incorporate strategic concepts into projects whilst guiding others.
Key Responsibilities
Medical Writing responsibilities
- Manage the preparation of regulatory documents e.g. CSRs, briefing documents, meeting requests, Clinical modules.
- Lead writing/editing of complex Clinical Dossiers/Safety Reports.
- Review documents to ensure compliance with documentation quality standards and regulatory requirements.
- Plan and create timelines to produce assigned documents.
Project Delivery
- Able to work across multiple projects and accounts simultaneously.
- Demonstrate a thorough understanding of timelines, budgetary constraints and scopes of work.
Communication
- Understand the purpose and role of communications in the wider therapy area and commercial landscape.
- Demonstrate the ability to communicate clearly to different audiences through a variety of media (print and digital).
Qualifications
- Life sciences degree, preferably MSc or PhD.
- Strong medical writing experience in either a CRO or pharmaceutical company.
- Substantial knowledge of varied therapeutic areas, regulatory/scientific guidelines and key statistical concepts.
- Experienced writer of clinical protocols (IS and NIS), study reports (IS and NIS), regulatory dossier level documents.
- RWE medical writing experience is an advantage.
- Previous experience in a medical communications agency or industry is also considered.
- English fluency.
If you feel that this could be the right next step for you, we would be delighted to engage with your application.
Ipsen is committed to fostering a diverse and inclusive workplace where all employees feel valued and empowered.
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