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Clinical Trial Manager(m/w/x)
End-to-end protocol implementation and budget management for global therapeutic studies at a clinical research organization with 41,000+ employees. Prior monitoring experience and therapeutic area expertise preferred. Travel up to 20%, global employee assistance program.
Anforderungen
- Degree in medicine, science, or equivalent
- Ability to drive clinical study deliverables
- Expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
Aufgaben
- Plan and manage all clinical trial aspects
- Ensure adherence to timelines and budgets
- Maintain high quality standards
- Collaborate with cross-functional teams
- Establish and implement trial protocols
- Build relationships with investigators and stakeholders
- Ensure compliance with international and local regulations
- Adhere to ethical guidelines
- Make critical decisions on trial design
- Manage vendor selection and risk assessment
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Noch nicht perfekt?
- IQVIAVollzeitRemoteSeniorWienab 70.100 / Jahr
- ICON plc
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Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat
Clinical Trial Manager(m/w/x)
End-to-end protocol implementation and budget management for global therapeutic studies at a clinical research organization with 41,000+ employees. Prior monitoring experience and therapeutic area expertise preferred. Travel up to 20%, global employee assistance program.
Anforderungen
- Degree in medicine, science, or equivalent
- Ability to drive clinical study deliverables
- Expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
Aufgaben
- Plan and manage all clinical trial aspects
- Ensure adherence to timelines and budgets
- Maintain high quality standards
- Collaborate with cross-functional teams
- Establish and implement trial protocols
- Build relationships with investigators and stakeholders
- Ensure compliance with international and local regulations
- Adhere to ethical guidelines
- Make critical decisions on trial design
- Manage vendor selection and risk assessment
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Über das Unternehmen
ICON plc
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Noch nicht perfekt?
- IQVIA
Local Trial Manager - Sponsor Dedicated(m/w/x)
VollzeitRemoteSeniorWienab 70.100 / Jahr - ICON plc
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Vollzeitmit HomeofficeBerufserfahrenWien - ICON plc
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorWien - 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