IQVIA
Clinical Research Associate I or II(m/w/x)
Vollzeitmit HomeofficeJunior
Wien
ab 3.600 / Monat
Neuer Job?Nejo!
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PSPSI CRO
Site Identification Specialist(m/w/x)
Wien
ab 70.000 / Jahr
Vollzeitmit HomeofficeJunior
Nejo KI-Zusammenfassung
Strategic relationship building and database refinement for clinical trial center selection at global CRO. University degree in MD or PharmD and advanced English skills required. On-site monitoring experience preferred.
Anforderungen
- University/college degree (MD/PharmD) or equivalent education, training, and experience
- On-site monitoring experience (plus)
- Understanding of Good Clinical Practice, local laws, and regulations
- Ability to work in dynamic environment, under compressed deadlines
- Advanced English skills
Aufgaben
- Communicate with clinical sites
- Build relationships with clinical sites
- Identify potential centers for clinical trials
- Maintain and refine internal site databases with cross-functional teams
- Conduct site identification activities during startup
- Discuss clinical trial protocols
- Collect site identification questionnaires
- Define study objectives and optimal site profiles
- Create initial lists of potential sites
- Refine site contact strategy with project teams
- Refine site contact methodology with project teams
- Maintain study site identification tracker with the project team
- Evaluate site identification progress with project teams
- Identify and highlight risks to timelines or objectives
- Conduct due diligence checks with Legal
- Evaluate regulatory and legal limitations for sites
- Evaluate regulatory and legal limitations for investigators
- Support project teams during study startup
- Provide support for additional site identification rounds
- Gather additional site or investigator information
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- Fair and attractive salary
Sonstige Vorteile
- Excellent working conditions
Lockere Unternehmenskultur
- Supportive and collaborative environment
- Friendly, professional team
Weiterbildungsangebote
- Extensive training
Karriere- und Weiterentwicklung
- 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?
- IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 4.200 / Monat - IQVIA Biotech
Clinical Associate Regulatory Submissions(m/w/x)
Vollzeitmit HomeofficeJuniorWien - AOP Health
Clinical Site Management Lead(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat
PSPSI CRO
Site Identification Specialist(m/w/x)
Wien
ab 70.000 / Jahr
Vollzeitmit HomeofficeJunior
Nejo KI-Zusammenfassung
Strategic relationship building and database refinement for clinical trial center selection at global CRO. University degree in MD or PharmD and advanced English skills required. On-site monitoring experience preferred.
Anforderungen
- University/college degree (MD/PharmD) or equivalent education, training, and experience
- On-site monitoring experience (plus)
- Understanding of Good Clinical Practice, local laws, and regulations
- Ability to work in dynamic environment, under compressed deadlines
- Advanced English skills
Aufgaben
- Communicate with clinical sites
- Build relationships with clinical sites
- Identify potential centers for clinical trials
- Maintain and refine internal site databases with cross-functional teams
- Conduct site identification activities during startup
- Discuss clinical trial protocols
- Collect site identification questionnaires
- Define study objectives and optimal site profiles
- Create initial lists of potential sites
- Refine site contact strategy with project teams
- Refine site contact methodology with project teams
- Maintain study site identification tracker with the project team
- Evaluate site identification progress with project teams
- Identify and highlight risks to timelines or objectives
- Conduct due diligence checks with Legal
- Evaluate regulatory and legal limitations for sites
- Evaluate regulatory and legal limitations for investigators
- Support project teams during study startup
- Provide support for additional site identification rounds
- Gather additional site or investigator information
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- Fair and attractive salary
Sonstige Vorteile
- Excellent working conditions
Lockere Unternehmenskultur
- Supportive and collaborative environment
- Friendly, professional team
Weiterbildungsangebote
- Extensive training
Karriere- und Weiterentwicklung
- 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
Research
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?
- IQVIA
Clinical Research Associate I or II(m/w/x)
Vollzeitmit HomeofficeJuniorWienab 3.600 / Monat - IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 4.200 / Monat - IQVIA Biotech
Clinical Associate Regulatory Submissions(m/w/x)
Vollzeitmit HomeofficeJuniorWien - AOP Health
Clinical Site Management Lead(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat