.At EVERSANA, we are proud to be certified as a Great Place to Work across the globe.
We're fueled by our vision to create a healthier world.
How?
Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry.
We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies.
Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them.
Our jobs, skills and talents are unique, but together we make an impact every day.
Join us!Across our growing organization, we embrace diversity in backgrounds and experiences.
Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry.
We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs.
We are deliberate and self-reflective about the kind of team and culture we are building.
We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve.
We are EVERSANA.Job DescriptionTHE POSITION:The Medical, Legal and Regulatory (MLR) review is an essential process in healthcare marketing to make sure advertising, promotional and non-promotional content is accurate, compliant, and ready to be published.
The MLR process must rigorously control and execute review, approval and document filing actions.
As part of the MLR team, the Medical Content and Review Specialist is responsible for managing all the MLR process for a dedicated client.
The Medical Content and Review Specialist ensures that all administrative and program management support for the client's MLR process operates effectively and in full compliance with all internal and external policies and regulations.The role is home office based, (full-time position), ideally located in Poland, Germany, Ireland, the UK, Italy, Portugal, or Spain and the job holder must be legally eligible to work in the European Union or the UK.Essential Duties And ResponsibilitiesOur employees are tasked with delivering excellent business results through the efforts of their teams.
These results are achieved by:Medical Content And Review Specialist ResponsibilitiesManages the end-to-end MLR process.Responsible for scheduling, setting the agenda, and leading Review Committee meetings.Add live discussion notes for comments discussed in Veeva VaultScribe meeting minutes, circulate draft meeting minutes for Committee approval and finalize and file approved minutesEnsure all covered communications are properly vetted through the review process utilizing the online review system (e.G