Dein persönlicher KI-Karriere-Agent
(Senior) Clinical Trial Assistant(m/w/x)
Supporting clinical trial management at a global CRO, handling documentation and coordinating meetings. Extensive clinical trial support experience required. 4 weeks vacation, health insurance, retirement planning.
Anforderungen
- Strong foundation in clinical trial management
- Ability to work independently and guide others
- Bachelor's degree in relevant scientific or healthcare field
- Extensive experience in clinical trial support
- Solid understanding of clinical trial processes
- Solid understanding of regulatory requirements
- Strong organizational skills
- Strong multitasking skills
- Ability to manage multiple tasks and projects effectively
- Proficiency in clinical trial management systems
- Proficiency in relevant software
- Keen eye for detail in documentation
- Keen eye for detail in data management
- Excellent communication skills
- Excellent interpersonal skills
- Excellent problem-solving skills
- Ability to work collaboratively with diverse teams
- Ability to work collaboratively with diverse stakeholders
- Willingness to travel as required
- Travel approximately 10%
- Encouraged to apply even if not all requirements met
Aufgaben
- Support clinical trial management
- Handle administrative tasks
- Manage clinical trial documentation
- Coordinate meetings
- Maintain trial-related records
- Prepare regulatory documents
- Submit regulatory documents
- Ensure compliance with study protocols
- Ensure regulatory compliance
- Collaborate with cross-functional teams
- Support trial operations
- Resolve trial issues
- Monitor trial progress
- Track trial progress
- Manage site communications
- Ensure timely delivery of study materials
- Build relationships with site staff
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
- Support project success
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial management systems
- relevant software
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
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Noch nicht perfekt?
- ICON plcVollzeitRemoteBerufserfahrenFrankfurt am Main
- IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main, Hamburg - ICON plc
Clinical Research Lead Assistant(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main
(Senior) Clinical Trial Assistant(m/w/x)
Supporting clinical trial management at a global CRO, handling documentation and coordinating meetings. Extensive clinical trial support experience required. 4 weeks vacation, health insurance, retirement planning.
Anforderungen
- Strong foundation in clinical trial management
- Ability to work independently and guide others
- Bachelor's degree in relevant scientific or healthcare field
- Extensive experience in clinical trial support
- Solid understanding of clinical trial processes
- Solid understanding of regulatory requirements
- Strong organizational skills
- Strong multitasking skills
- Ability to manage multiple tasks and projects effectively
- Proficiency in clinical trial management systems
- Proficiency in relevant software
- Keen eye for detail in documentation
- Keen eye for detail in data management
- Excellent communication skills
- Excellent interpersonal skills
- Excellent problem-solving skills
- Ability to work collaboratively with diverse teams
- Ability to work collaboratively with diverse stakeholders
- Willingness to travel as required
- Travel approximately 10%
- Encouraged to apply even if not all requirements met
Aufgaben
- Support clinical trial management
- Handle administrative tasks
- Manage clinical trial documentation
- Coordinate meetings
- Maintain trial-related records
- Prepare regulatory documents
- Submit regulatory documents
- Ensure compliance with study protocols
- Ensure regulatory compliance
- Collaborate with cross-functional teams
- Support trial operations
- Resolve trial issues
- Monitor trial progress
- Track trial progress
- Manage site communications
- Ensure timely delivery of study materials
- Build relationships with site staff
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
- Support project success
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial management systems
- relevant software
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
- 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?
- ICON plc
Clinical Trial Assistant(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main, Hamburg - ICON plc
Clinical Research Lead Assistant(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main