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: Spain, 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 At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled