(Sr.) Medical Review Manager Germany (m/f/d)
PfizerAbout the role
A career at Pfizer offers opportunity, ownership and impact.
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.
Right now, we are seeking highly qualified candidates to fill the position:
(Sr.) Medical Review Manager Germany (m/f/d)
About the role:
Strategic oversight:
Subject Matter Expert and single point of contact for Medical Review to enable lightspeed deliverables for Promotional & Medical-to-Medical review objectives for Medical.
Identify strategic opportunities for in-country service and operations improvements that align with business priorities & building consensus among cross-functional teams and influence decision making.
Gather and analyze in-country metrics focused on utilization and performance; develop compelling and insightful strategic recommendations for leadership and the country.
Close partnership with CMAO categories, and country partners to drive active engagement with key Medical and Marketing stakeholders.
Leads process documentation and improvement, as applicable.
Provision of Medical Expertise in Relation to Content of Materials
To acquire and maintain in-depth scientific knowledge of Pfizer medicines within nominated therapy area(s) (including those in development) as well as the competitive landscape.
To understand and advocate the appropriate use of medicines with the local health system.
Collaboration with Pfizer teams to Enable Streamlined Content Creation:
Works with the nominated cross functional team(s) in-country and above-country to develop impactful and compliant promotional and non-promotional materials of value to healthcare professionals and patients. This includes for example:
advising on marketing programmes, other promotional activities and medical education
providing support for revisions to prescribing information and implementation of risk management plans
working with digital materials and digital technologies
collaborating with Medical Affairs colleagues to understand therapy area and share pertinent issues with the relevant teams
Provides specialist medical, scientific and code/regulatory advice to teams during the development phase of materials/projects/activities to support streamlined creation of compliant content/activities that enable appropriate use of Pfizer medicines and successful implementation of materials, initiatives and programmes for example:
advising on and reviewing materials for submission to health authorities
advising on and reviewing materials for package deals and materials for patient support
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