IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare.
In your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and, ultimately, improve outcomes for patients.
IQVIA offers a competitive salary and great benefits, including a profit-related annual bonus, paid leave, and private health insurance.
Forge a career with greater purpose, make an impact, and never stop learning"
If you are looking to take your medical writing career to the next level as a manager in our team, we will provide you with opportunities to manage programs of studies, build and maintain relationships with key customers, and oversee the training and onboarding of teams.
You will be able to develop your career in our team along either a management or technical route depending on your preference.
We are looking for a lead Medical Writer who is capable of leading on a wide variety of writing projects, using their best judgment and experience from working on programmes of studies.
You will be the point of contact for issues and escalation and will be expected to design and deliver training sessions.
Initially there will not be any direct line management of others.
Acting as Lead Medical Writer, on projects with multiple deliverables / components. Preparing assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines.
You will be comfortable performing senior review of all types of medical writing deliverables, providing feedback and guidance to junior staff, negotiates timelines and discusses / resolves customer comments.
You will be responsible for keeping up to date with current writing / regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development writing.
Do you meet the skills, experience, and educational requirements of this role?
Confidence in appropriately challenging the customer when document quality or timelines are at risk.
At IQVIA, 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.
The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at .
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