Posted:
8/5/2024, 5:00:00 PM
Location(s):
England, United Kingdom ⋅ London, England, United Kingdom
Experience Level(s):
Senior
Field(s):
Medical, Clinical & Veterinary
Reporting directly to the Account Lead and indirectly to the Account Manager, you’ll ensure that the Quality Control 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 technical review and or deputise for the account manager in their absence.
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.)
Attend account WIP meetings to assign tasks/escalate issues
Responsible for the Quality Control (second review) of customer materials.
Provide technical (first) review of materials as account requires.
Deputise for AM in their absence
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/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 advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
Website: https://iqvia.com/
Headquarter Location: Danbury, Connecticut, United States
Employee Count: 10001+
Year Founded: 1982
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Analytics ⋅ Health Care ⋅ Life Science