Dein persönlicher KI-Karriere-Agent
Clinical Trial Associate(m/w/x)
Assisting with clinical trial coordination and documentation for a global CRO. Bachelor's degree and knowledge of trial processes required. Annual leave entitlements, health insurance, and retirement planning.
Anforderungen
- Bachelor's degree in scientific/healthcare field
- Clinical research experience or strong interest
- Knowledge of clinical trial processes, regulations, guidelines
- Excellent organizational and communication skills
- Collaborative work in fast-paced environment
- Attention to detail
- Willingness to travel approximately 10%
- Fluency in German and English language
Aufgaben
- Assist in clinical trial coordination and administration
- Ensure compliance with protocols and regulatory requirements
- Maintain and organize clinical trial documentation
- Prepare study-related materials like informed consent forms
- Support cross-functional team communication
- Track and report clinical trial metrics and milestones
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- 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
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Gefällt dir diese Stelle?
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Clinical Trial Associate(m/w/x)
Assisting with clinical trial coordination and documentation for a global CRO. Bachelor's degree and knowledge of trial processes required. Annual leave entitlements, health insurance, and retirement planning.
Anforderungen
- Bachelor's degree in scientific/healthcare field
- Clinical research experience or strong interest
- Knowledge of clinical trial processes, regulations, guidelines
- Excellent organizational and communication skills
- Collaborative work in fast-paced environment
- Attention to detail
- Willingness to travel approximately 10%
- Fluency in German and English language
Aufgaben
- Assist in clinical trial coordination and administration
- Ensure compliance with protocols and regulatory requirements
- Maintain and organize clinical trial documentation
- Prepare study-related materials like informed consent forms
- Support cross-functional team communication
- Track and report clinical trial metrics and milestones
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- 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
- 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
ICON Clinical Research Germany GmbH
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
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