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Science Team Lead, Collaborative, Royal Tunbridge Wells
Company overview
An IQVIA business, publishes Medthority (), which provides a trusted and compliant decision support tool for healthcare professionals, offering curated content from prescription medicines insights to clinical trial highlights and treatment guidelines. The platform features disease-specific Learning Zones, supporting healthcare education sponsored by pharmaceutical partners.
Role overview:
Are you an experienced medical writer and reviewer with a proven track record in managing people and client interactions? Can you:
* Review and edit content to ensure discoverability, ABPI compliance, and ease of understanding for busy healthcare professionals?
* Support content that encourages engagement and behavior change?
* Manage challenging client relationships to achieve optimal outcomes for clients, teams, and HCP users?
* Plan resources, including freelancers, to deliver content on time and within budget, maintaining work–life balance?
* Oversee a team of in-house and freelance writers, providing mentoring and feedback?
Responsibilities:
* Oversee medical writers and collaborate with the editorial team and other departments to understand business opportunities, support proposal development, and ensure content compliance, including ABPI standards.
* Review work to ensure medical accuracy, engagement, compliance, and suitability for an HCP audience, providing developmental feedback.
* Participate in client meetings to understand priorities, contribute ideas, and demonstrate scientific credibility.
* Support ongoing client discussions to address challenges and solutions.
* Manage your workload and that of your team across multiple proposals, coordinating with commercial and sales teams, and allocating resources as needed.
* Innovate to expand the scope and value of Medthority content.
* Contribute to improving workflows, processes, standards, and mentor medical writers.
Qualifications and skills:
* UK citizen or resident with right to work in the UK.
* BSc or higher in biomedical science; relevant industry experience may substitute for degree.
* Experience in medical communications, journalism, strategy, consulting, or medical affairs within the pharmaceutical industry.
* Line management experience overseeing medical writers, in-house or remote.
* Client-facing experience with the ability to manage challenging relationships.
* Experience with grants and proposals is a plus.
* Strong scientific communication skills, with the ability to edit and adapt content across styles.
* Ability to learn new therapy areas quickly and handle multiple projects.
* Understanding of drug development and relevant regulations for communicating with healthcare professionals and the public.
* Ability to incorporate feedback and maintain high standards.
* Creative problem-solving skills.
* Strong project and time management skills.
* Flexible, proactive, able to multi-task, adapt quickly, and work under pressure.
* Excellent interpersonal and communication skills, capable of working independently and in dispersed teams.
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