Boehringer Ingelheim
Postdoc - Evidence Synthesis for Decision Making in HTA & MA(m/w/x)
Vollzeit
mit Homeoffice
Berufserfahren
Keine Angabe
Ingelheim am Rhein, Biberach
AB
AbbVie10 Tage
Joint Clinical Assessment (JCA) Dossier Manager, International HTA Strategy(m/w/x)
Vollzeit
mit Homeoffice
Senior
Keine Angabe
Wiesbaden
Nejo KI-Zusammenfassung
In this role, you will lead the JCA dossier process, ensuring compliance with EUHTA regulations while coordinating cross-functional teams. Your day-to-day responsibilities will include conducting strategic workshops, communicating effectively with stakeholders, and driving project success within budget and timelines.
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Anforderungen
- •At least 8 years of experience
- •Bachelor’s degree or advanced degree in life sciences, health service, or related discipline
- •Understanding of pricing and reimbursement processes for key HTA markets
- •Experience with AMNOG, HAS, NICE, CDA dossier submissions
- •Understanding of evidence synthesis concepts
- •Proven experience managing projects in the pharmaceutical industry
- •Strong knowledge of project management software and tools
- •Excellent leadership, interpersonal, and communication skills
- •Strong ability in working collaboratively across matrix functions
- •Ability to work independently and make informed decisions
Bachelor-Abschluss
ODER
Master-Abschluss
Berufserfahrung
8 Jahre
Deine Aufgaben
- •Lead the end-to-end JCA dossier process
- •Provide expertise in EUHTA regulations
- •Serve as an EU HTA dossier expert for the team
- •Ensure timely and budget-compliant execution of JCA procedural steps
- •Achieve project objectives while adhering to quality standards
- •Act as a liaison to HTA external authorities
- •Support all Therapeutic Areas and European countries as the JCA dossier expert
- •Shape internal operational processes in response to new EU HTA requirements
- •Conduct resource evaluations for the JCA dossier teams
- •Arrange and lead JCA Strategy Workshops
- •Develop meeting minutes and action plans from workshops
- •Communicate effectively with the JCA Dossier team and stakeholders
- •Develop project plans, timelines, budgets, and vendor evaluations
- •Coordinate cross-functional teams including Access Lead and Medical Affairs
- •Oversee evidence retrieval activities for dossier integration
- •Ensure compliance with EUHTA regulations and quality standards
- •Identify key risks and propose mitigation strategies
- •Contribute to establishing frameworks for EUHTA Regulation implementation
- •Recommend and implement process improvements and best practices
Sprachen
Englisch – verhandlungssicher
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