Senior Medical Writer II - Brand & Promotion
New
A
AQ International Medical Communications Agency
United KingdomFull-TimeSenior
Salary not disclosed
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Job Details
- Experience
- Minimum 4 years’ experience
- Required Skills
- Microsoft ExcelMicrosoft OfficePowerPoint
Requirements
- PhD in a scientific discipline
- Minimum 4 years’ experience in medical writing
- Experience within a medical communications agency
- Strong emphasis on pharmaceutical promotional materials
- Expertise in developing Brand Campaigns, Brand Narratives, Detail Aids, Leave Pieces, emails, digital promotional content, and congress materials
- In-depth understanding and practical application of the ABPI Code of Practice
- Proficiency in Microsoft Office (Word®, PowerPoint®, Excel®)
- Proficiency in Adobe Acrobat®
- Proficiency in reference-management tools (e.g., EndNote®)
- Experienced with literature databases (e.g., PubMed)
- Ability to master new therapeutic areas quickly
- Ability to communicate clearly and persuasively
- Willingness to travel occasionally for client meetings and live events
Responsibilities
- Produce high-quality promotional content that is scientifically robust, strategically aligned, and brand consistent.
- Develop and refine copy for a range of promotional deliverables including Promotional Campaigns, Detail Aids, and promotional emails.
- Apply a strong understanding of the ABPI Code of Practice and ensure all materials meet compliance requirements.
- Interpret complex scientific data and translate it into clear, credible, and compelling promotional messages.
- Conduct targeted literature searches to identify data that strengthen brand messaging, claims, and promotional narratives.
- Develop multiple rounds of content with precision, including annotations, references, claims support, and ABPI-compliant substantiation.
- Collaborate closely with Account, Editorial, Creative, Digital, and Client Services teams to ensure timely, cohesive delivery.
- Manage multiple priorities efficiently, delivering work within allocated budgeted hours and communicating proactively around timelines.
- Lead scientific discussions with clients and external experts in calls, meetings, and medical-legal-regulatory (MLR) review sessions.
- Navigate and lead the MLR process confidently, providing scientific justification for claims and guiding internal teams.
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