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Clinical Research Lead Assistant(m/w/x)
Administrative support for clinical trials documentation and regulatory submissions at global healthcare intelligence organization. Extensive clinical trial support experience and CTMS proficiency required. Involvement in international clinical research projects.
Anforderungen
- Advanced degree or certification in relevant field
- Extensive clinical trial support experience
- Understanding of clinical trial processes
- Strong organizational and multitasking skills
- Proficiency in clinical trial management systems
- Attention to detail in documentation
- Excellent communication and interpersonal skills
- Strong problem-solving skills
Aufgaben
- Provide administrative support for clinical trials
- Manage documentation and trial-related records
- Coordinate and schedule project meetings
- Prepare and submit regulatory documents
- Ensure compliance with protocols and requirements
- Collaborate with cross-functional teams
- Resolve operational issues during studies
- Monitor and track trial progress
- Manage communications with clinical sites
- Ensure timely delivery of study materials
- Build relationships with site staff and stakeholders
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Clinical trial management systems
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?
- ICON plcVollzeitRemoteBerufserfahrenFrankfurt am Main
- ICON plc
Senior Clinical Research Associate(m/w/x)
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Clinical Site Manager(m/w/x)
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Senior CRA (Sponsor dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main
Clinical Research Lead Assistant(m/w/x)
Administrative support for clinical trials documentation and regulatory submissions at global healthcare intelligence organization. Extensive clinical trial support experience and CTMS proficiency required. Involvement in international clinical research projects.
Anforderungen
- Advanced degree or certification in relevant field
- Extensive clinical trial support experience
- Understanding of clinical trial processes
- Strong organizational and multitasking skills
- Proficiency in clinical trial management systems
- Attention to detail in documentation
- Excellent communication and interpersonal skills
- Strong problem-solving skills
Aufgaben
- Provide administrative support for clinical trials
- Manage documentation and trial-related records
- Coordinate and schedule project meetings
- Prepare and submit regulatory documents
- Ensure compliance with protocols and requirements
- Collaborate with cross-functional teams
- Resolve operational issues during studies
- Monitor and track trial progress
- Manage communications with clinical sites
- Ensure timely delivery of study materials
- Build relationships with site staff and stakeholders
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Clinical trial management systems
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?
- ICON plc
Clinical Trial Assistant(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - ICON plc
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Site Manager(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main