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. #J-18808-Ljbffr
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. #J-18808-Ljbffr
