AOP Health
Manager Medical Information(m/w/x)
Vollzeitmit HomeofficeSenior
Wien
ab 45.080 / Jahr
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
BOBoehringer Ingelheim
Study Physician(m/w/x)
Wien
ab 108.000 / Jahr
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Medical oversight of clinical trial protocols and data review for global pharmaceutical research. Specialization in Internal Medicine or General Practice with industry experience required. Additional bridge-days off and subsidized staff restaurant.
Anforderungen
- Medical degree with clinical training
- At least 4 years clinical practice
- Specialization in Internal Medicine or General Practice
- Experience in pharmaceutical industry or CRO
- Understanding of ICH-GCP and clinical research
- Strong analytical and communication skills
- Structured working style and international collaboration
- Proficiency in medical data review
- Fluency in English
Aufgaben
- Provide end-to-end medical support throughout the study lifecycle
- Ensure high-quality medical content in clinical trial protocols
- Collaborate with cross-functional stakeholders on trial development
- Develop the Clinical Quality Monitoring Plan
- Conduct ongoing medical data reviews
- Support risk-based quality management
- Define key protocol deviations
- Provide medical input for investigator and team trainings
- Advise on eCRF design and automated data checks
- Review ICFs, lab alerts, and recruitment activities
- Contribute to regulatory and ethics committee responses
- Address medical questions from investigators
- Support adjudication and Data Monitoring Committee processes
- Provide state-of-the-art medical expertise to project teams
- Execute medical oversight during trial preparation and conduct
- Manage medical reporting for clinical trials
- Serve as a core member of the Trial Team
- Participate in the Evidence Network for the asset
Berufserfahrung
- 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- ICH-GCP regulations
Benefits
Flexibles Arbeiten
- Home office
- Flexible working hours
- Flexible working time models
Mehr Urlaubstage
- Additional bridge-days off
Gratis oder Vergünstigte Mahlzeiten
- Subsidized staff restaurant
- Subsidized cafeteria
- Vegetarian and vegan options
Weiterbildungsangebote
- Learning and development opportunities
Gesundheits- & Fitnessangebote
- Health promotion programs
Öffi Tickets
- Public transport ticket coverage
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Boehringer Ingelheim erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- AOP Health
Clinical Site Management Lead(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA
Local Trial Manager - Sponsor Dedicated(m/w/x)
VollzeitRemoteSeniorWienab 70.100 / Jahr - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat - AstraZeneca
Medical Science Liaison – CVRM(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 69.488,8 / Jahr
BOBoehringer Ingelheim
Study Physician(m/w/x)
Wien
ab 108.000 / Jahr
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Medical oversight of clinical trial protocols and data review for global pharmaceutical research. Specialization in Internal Medicine or General Practice with industry experience required. Additional bridge-days off and subsidized staff restaurant.
Anforderungen
- Medical degree with clinical training
- At least 4 years clinical practice
- Specialization in Internal Medicine or General Practice
- Experience in pharmaceutical industry or CRO
- Understanding of ICH-GCP and clinical research
- Strong analytical and communication skills
- Structured working style and international collaboration
- Proficiency in medical data review
- Fluency in English
Aufgaben
- Provide end-to-end medical support throughout the study lifecycle
- Ensure high-quality medical content in clinical trial protocols
- Collaborate with cross-functional stakeholders on trial development
- Develop the Clinical Quality Monitoring Plan
- Conduct ongoing medical data reviews
- Support risk-based quality management
- Define key protocol deviations
- Provide medical input for investigator and team trainings
- Advise on eCRF design and automated data checks
- Review ICFs, lab alerts, and recruitment activities
- Contribute to regulatory and ethics committee responses
- Address medical questions from investigators
- Support adjudication and Data Monitoring Committee processes
- Provide state-of-the-art medical expertise to project teams
- Execute medical oversight during trial preparation and conduct
- Manage medical reporting for clinical trials
- Serve as a core member of the Trial Team
- Participate in the Evidence Network for the asset
Berufserfahrung
- 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- ICH-GCP regulations
Benefits
Flexibles Arbeiten
- Home office
- Flexible working hours
- Flexible working time models
Mehr Urlaubstage
- Additional bridge-days off
Gratis oder Vergünstigte Mahlzeiten
- Subsidized staff restaurant
- Subsidized cafeteria
- Vegetarian and vegan options
Weiterbildungsangebote
- Learning and development opportunities
Gesundheits- & Fitnessangebote
- Health promotion programs
Öffi Tickets
- Public transport ticket coverage
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Boehringer Ingelheim erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Boehringer Ingelheim
Branche
Pharmaceuticals
Beschreibung
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
Noch nicht perfekt?
- AOP Health
Manager Medical Information(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - AOP Health
Clinical Site Management Lead(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA
Local Trial Manager - Sponsor Dedicated(m/w/x)
VollzeitRemoteSeniorWienab 70.100 / Jahr - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat - AstraZeneca
Medical Science Liaison – CVRM(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 69.488,8 / Jahr