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Manager, Medical Writer - Evidence Generation & Value Communications
2 days ago
Recruiting.com
career sites • recruiting software • employment brand • candidate relationship management • talent community
Description
• Under the general direction of the Team Lead for Global Dossiers, and in close collaboration with team members across the Evidence Generation & Value Communications service line, you will play a critical role in developing scientific and medical content that helps pharmaceutical, biotech, and device technologies to successfully commercialize innovative medical treatments and technologies in complex and cost-constrained global markets. • As a Manager, you would be responsible for client management, content development and/or content review (~70% of duties). • As the primary point of contact for clients, you will ensure projects are delivered on time, on budget and to the client’s satisfaction. • A substantial part of the role involves content development and/or review for Evidence Generation & Value Communications deliverables including (but not limited to): global value dossiers (GVDs), country-level submission documents, targeted literature reviews, abstracts and posters for presentation, peer-reviewed publications, and Microsoft PowerPoint slide decks. • There will also be opportunities to contribute to new business development, ie identifying potential follow-on work, developing proposals and drafting budgets for new work. • This role offers the chance for a motivated market access writer with an understanding of value communications in a consulting setting looking to move to the next level to join our dynamic team of experienced, detail-orientated writers and researchers to produce high-quality deliverables that are aligned with Cencora’s core mission and vision.
Requirements
• Advanced degree in clinical, life sciences or related scientific discipline is preferred; • 2–3 years practical experience in a relevant market access or medical writing role, ideally within an agency/consulting setting • Excellent verbal and written communication skills, as well as demonstrating a professional etiquette towards both colleagues and clients to foster a positive and inclusive work environment based on respect and collaboration • High attention to detail and experience with fact-checking and copy-editing • Passion for writing with a high attention to detail; agility to pivot easily between different projects and ability to become familiar with new topics quickly. • Familiarity with presenting complex scientific literature, clinical trial data, health economics studies and real-world evidence in a straightforward, accurate manner • Strong project management skills, including the ability to organize, prioritize, and maintain high quality work output in a fast-paced dynamic environment while working on multiple projects • Knowledge of the pharmaceutical industry, global market access, and health technology assessments (HTAs) • Proficiency with Microsoft Office Suite (Word, PowerPoint, Excel) and associated software (e.g. EndNote)
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