Dein persönlicher KI-Karriere-Agent
Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Sponsor-dedicated clinical trial monitoring and site initiation for a global CRO. Minimum 2 years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, health insurance, retirement planning.
Anforderungen
- Relevant clinical trial monitoring experience
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills, attention to detail
- Ability to work independently and collaboratively
- Ability to work in fast-paced environment
- Willingness to travel as required (approx. 60%)
Aufgaben
- Design and analyze clinical trials
- Interpret complex medical data
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial sites
- Close out clinical trial sites
- Ensure protocol compliance
- Maintain data integrity
- Safeguard patient safety
- Collaborate with investigators
- Work with site staff
- Review clinical data
- Resolve data queries
- Prepare study documentation
- Review study documentation
- Contribute to clinical study reports
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Sonstige Zulagen
- Flexible country-specific optional benefits
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
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Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Sponsor-dedicated clinical trial monitoring and site initiation for a global CRO. Minimum 2 years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, health insurance, retirement planning.
Anforderungen
- Relevant clinical trial monitoring experience
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills, attention to detail
- Ability to work independently and collaboratively
- Ability to work in fast-paced environment
- Willingness to travel as required (approx. 60%)
Aufgaben
- Design and analyze clinical trials
- Interpret complex medical data
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial sites
- Close out clinical trial sites
- Ensure protocol compliance
- Maintain data integrity
- Safeguard patient safety
- Collaborate with investigators
- Work with site staff
- Review clinical data
- Resolve data queries
- Prepare study documentation
- Review study documentation
- Contribute to clinical study reports
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Sonstige Zulagen
- Flexible country-specific optional benefits
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
850 RPS Research Services Austria
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Noch nicht perfekt?
- ICON plc
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Vollzeitnur vor OrtBerufserfahrenWien - QAT IQVIA RDS Austria GmbH
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