Senior Medical Reviewer (Pharmareview)

As a Senior Medical Review, you will be part of a dynamic team, working across multiple different therapy areas with some of the leading pharmaceutical companies. You will review documents for scientific accuracy against applicable regional codes (ABPI, EFPIA, etc.). These documents are created by the client for marketing their products, including symposia materials, speaker slide decks, and social media posts.

This role suits individuals who have prior experience in copy review, medical writing, and medical affairs. You will be responsible for quality checking reviews performed by the account executive, providing feedback directly to them and their line manager.

This position offers a great opportunity to deepen your knowledge of the medical affairs industry and observe the future of the pharmaceutical landscape.

1. Ensure tasks are appropriately added to WIP from the customer review and approval system, with all tasks estimated (time to complete, TR, QC, etc.).
2. Ensure tasks are uploaded correctly to the task management system.
3. Attend account WIP meetings to assign tasks and escalate issues.
4. Attend team meetings to assign tasks and escalate issues.
5. Responsible for the Quality Control (second review) of customer materials.
6. Provide technical (first) review of materials against the appropriate country codes as required.
7. Deputise for the Account Manager in their absence by overseeing task assignments.
8. Maintain up-to-date knowledge of various therapeutic areas and client products; attend relevant training sessions.
9. Participate in monthly mentorship sessions led by medical leads on relevant topics.
10. Stay informed on updates to Codes of Practice (ABPI, IPHA, EFPIA, PhRMA).
11. Provide constructive coaching to Account Executives on technical review tasks and feedback on their development.

• Life science degree or equivalent.
• Experience working in the life sciences industry (pharmaceutical, medical device, healthcare agency, or similar).
• At least one year of experience in writing, managing, reviewing, or proofreading medical/scientific materials.
• High attention to detail.
• Excellent time management skills.
• Highly organized, capable of managing multiple tasks in a fast-paced environment.
• Excellent written and oral communication skills.
• Problem-solving skills and solution-oriented mindset.
• Experience with review and approval systems like Veeva Vault PromoMats, Aprimo, or similar.
• Fluency in English.
• Knowledge of applicable Codes of Practice, including ABPI, EFPIA, and PhRMA.
• Locations: UK, Spain, Portugal, Poland, Slovakia, and South Africa. Note: This role is not eligible for UK visa sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. Learn more at .