Senior Medical Reviewer (Pharmareview)
Senior Medical Reviewer (Pharmareview)
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Job Description
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 previously worked 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
Role and responsibilities
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 EFPIAPhRMA) including any updates.
Provide constructive coaching to AEs on technical review tasks. Provide feedback to AM/AL on AEs 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/copy reviewing/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 ABPI Code 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
Required Experience:
Senior IC
Employment Type
Full-Time
