Boehringer Ingelheim
Study Physician(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Wien
ab 108.000 / Jahr
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
PSPSI CRO
Medical Monitor (Gastroenterology)(m/w/x)
Wien
ab 80.000 / Jahr
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Medical oversight for global GI clinical trials, advising teams and sponsors on patient safety. Gastroenterology fellowship and 10+ years MD experience required. Research experience a plus, with 6 weeks vacation.
Anforderungen
- Medical Doctor degree
- Gastroenterology Fellowship certification
- Minimum 10 years practicing MD experience
- Research and/or industry experience (plus)
- Full working English proficiency
- MS Office applications proficiency
- Communication, presentation, and analytical skills
- Teamwork, problem-solving, detail-oriented
Aufgaben
- Provide medical input to global clinical studies
- Advise teams and business partners on medical matters
- Focus on patient safety and well-being
- Serve as medical point of contact for internal teams, study sites, and sponsors
- Advise clients, project teams, sites, regulatory agencies, and vendors on medical matters
- Collaborate on clinical development plans
- Collaborate on protocols
- Collaborate on investigator brochures
- Collaborate on annual reports
- Collaborate on clinical study reports
- Collaborate on patient narratives
- Collaborate on scientific presentations
- Review and analyze clinical data for participant safety
- Ensure trial data is accurate, complete, and verifiable
- Ensure trial conduct complies with approved protocol/amendments
- Address safety issues across the trial from sites and study teams
- Support medical data review
- Participate in bid defense meetings
- Participate in proposal activities
- Assist in pharmacovigilance activities
- Identify trial risks
- Create mitigation strategies
- Implement mitigation strategies with relevant departments
- Organize clinical development advisory boards
- Lead clinical development advisory boards
- Organize safety monitoring boards
- Lead safety monitoring boards
- Ensure study team compliance with FDA, EMEA, ICH, and GCP guidelines
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
Benefits
Sonstige Vorteile
- Excellent working conditions
Weiterbildungsangebote
- Extensive training
Lockere Unternehmenskultur
- Friendly team
Mentoring & Coaching
- Personal and professional growth opportunities
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens PSI CRO 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?
- ICON plc
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorWien - AOP Health
Manager Medical Information(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - ICON plc
Sr. Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWien - IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 4.200 / Monat
PSPSI CRO
Medical Monitor (Gastroenterology)(m/w/x)
Wien
ab 80.000 / Jahr
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Medical oversight for global GI clinical trials, advising teams and sponsors on patient safety. Gastroenterology fellowship and 10+ years MD experience required. Research experience a plus, with 6 weeks vacation.
Anforderungen
- Medical Doctor degree
- Gastroenterology Fellowship certification
- Minimum 10 years practicing MD experience
- Research and/or industry experience (plus)
- Full working English proficiency
- MS Office applications proficiency
- Communication, presentation, and analytical skills
- Teamwork, problem-solving, detail-oriented
Aufgaben
- Provide medical input to global clinical studies
- Advise teams and business partners on medical matters
- Focus on patient safety and well-being
- Serve as medical point of contact for internal teams, study sites, and sponsors
- Advise clients, project teams, sites, regulatory agencies, and vendors on medical matters
- Collaborate on clinical development plans
- Collaborate on protocols
- Collaborate on investigator brochures
- Collaborate on annual reports
- Collaborate on clinical study reports
- Collaborate on patient narratives
- Collaborate on scientific presentations
- Review and analyze clinical data for participant safety
- Ensure trial data is accurate, complete, and verifiable
- Ensure trial conduct complies with approved protocol/amendments
- Address safety issues across the trial from sites and study teams
- Support medical data review
- Participate in bid defense meetings
- Participate in proposal activities
- Assist in pharmacovigilance activities
- Identify trial risks
- Create mitigation strategies
- Implement mitigation strategies with relevant departments
- Organize clinical development advisory boards
- Lead clinical development advisory boards
- Organize safety monitoring boards
- Lead safety monitoring boards
- Ensure study team compliance with FDA, EMEA, ICH, and GCP guidelines
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
Benefits
Sonstige Vorteile
- Excellent working conditions
Weiterbildungsangebote
- Extensive training
Lockere Unternehmenskultur
- Friendly team
Mentoring & Coaching
- Personal and professional growth opportunities
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens PSI CRO 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
PSI CRO
Branche
Healthcare
Beschreibung
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Noch nicht perfekt?
- Boehringer Ingelheim
Study Physician(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 108.000 / Jahr - ICON plc
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorWien - AOP Health
Manager Medical Information(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - ICON plc
Sr. Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWien - IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 4.200 / Monat