Through our comprehensive training programme, you will become an expert reviewer, specializing in pharmaceutical industry compliance whilst also expanding your transferable skills. Reporting directly to the Account Lead and indirectly to the Account Manager, you’ll ensure that the Technical Review tasks assigned to you are completed on time and within budget. You’ll escalate task concerns or bottlenecks to the account/medical team in a timely manner. When needed you may be required to perform other account tasks to support the business.

Role and responsibilities

Responsible for the technical review (first review) of customer materials.

Ensure all 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.) and checked with the AM

Attend account WIP meetings to learn which tasks you will be responsible for completing, and escalate any concerns/issues

Provide account support on ancillary tasks as required

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.

Key requirements for role

Life science degree or equivalent

High levels of attention to detail

Excellent time management

Highly organised and enjoy working in fast-paced role working on many tasks

Excellent written and oral communication skills

A fundamental understanding of statistical analysis

Experience in problem-solving and providing solutions

Willingness to learn new skills

Fluency in English language

Desirable

Pharmacist or Medical Qualification

Signatory/AQP expertise

Life science masters or PhD (MSc, MRes, MPharm, MBBS, or PhD), ideally in a subject including human, disease and therapeutics

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

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

Preferably locations: UK, Spain and Portugal (South Africa, Poland and Slovakia)

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