Manager (Medical Writer), Evidence Generation & Value Communications (Global Dossiers)

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Requirements:

• Advanced degree in clinical, life sciences, or related scientific discipline preferred.
• 2–3 years practical experience in a relevant market access or medical writing role, ideally within an agency or consulting setting.
• Excellent verbal and written communication skills, with a professional attitude towards colleagues and clients.
• High attention to detail, with experience in fact-checking and copy-editing.
• Passion for writing and ability to quickly adapt to new topics.
• Familiarity with presenting complex scientific literature and clinical trial data accurately.
• Strong project management skills, capable of organizing and prioritizing multiple tasks in a fast-paced environment.
• Knowledge of the pharmaceutical industry, global market access, and health technology assessments.
• Proficiency with Microsoft Office Suite and related software.

Responsibilities:

• Work as the primary medical writer or reviewer for developing accurate content for global value dossiers and related market access deliverables.
• Act as the day-to-day point of contact for clients, overseeing project calls and managing project financials to keep track of scope and timelines.
• Conduct targeted literature searches to inform project work across various disease areas.
• Build and maintain client relationships, identifying opportunities for further projects.
• Collaborate within the team and adapt to feedback to meet project expectations.
• Manage workload to deliver projects on-time and on-budget while ensuring high-quality standards.
• Contribute to internal initiatives related to content marketing and thought leadership.