Global Medical Writing Manager

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs in the U.S. France and the U.K we tackle areas of high unmet medical need through research and innovation.

Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration excellence and impact. At Ipsen every individual is empowered to be their true selves grow and thrive alongside the companys success. Join us on our journey towards sustainable growth creating real impact on patients and society!

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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 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. If you feel that this could be the right next step for you we would be delighted to engage with your application.

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