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 be reviewing documents for scientific accuracy against the applicable regional codes (ABPI, EFPIA etc.). These documents will be created by the client for the purposes of marketing their products, for use as symposia materials, speaker slide decks and social media posts.

This role would suit individuals who have previouslyworked within copy review, medical writing and medical affairs. You will be responsible for the quality check of reviews performed by the account executive and provide feedback to them directly, as well as to their direct line manager.

This is a great way to further your knowledge of the medical affairs industry and get to see the future of the pharmaceutical landscape

Ensure tasks are appropriately added to WIP from the customers review and approval system and that all tasks are estimated (time to complete, TR, QC etc.)

Ensure tasks are appropriately uploaded to the task management system

Attend account WIP meetings to assign tasks/escalate issues

Attend account team meetings to assign tasks/escalate issues

Responsible for the Quality Control (second review) of customer materials. 

Provide technical (first) review of materials, against the appropriate country codes as account requires

Deputise for AM in their absence, by overseeing the assignment of tasks directly

Ensuring up-to-date knowledge regarding a variety of therapeutic areas and client products; attend relevant training

Attend monthly mentorship sessions held by medical leads on topics of interest

Maintaining up-to-date knowledge of Codes of practice (ABPI, IPHA, EFPIA,PhRMA) including any updates.

Provide constructive coaching to AE’s on technical review tasks. Provide feedback to AM/AL on AE’s development.

Key requirements

Life science degree or equivalent

Experience of working in life sciences industry, (pharmaceutical, medical device or healthcare agency or equivalent)

Minimum one years’ experience of writing/managing/copyreviewing/proofreading medical / scientific materials

High levels of attention to detail

Excellent time management

Highly organised and enjoy working in fast-paced role managing multiple tasks

Excellent written and oral communication skills

Experience in problem solving and providing solutions

Constructive feedback [people] skills

Experience working in Veeva Vault PromoMats/MedComms, Aprimo or similar review and approval system

Fluency in English language

Knowledge of the applicable Codes of practice, including ABPICode of Practice, EFPIA Code, PhRMA Code

Locations: UK, Spain, Portugal, Poland, Slovakia and South Africa. 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 help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com