Die KI-Suchmaschine für Jobs
Clinical Trial Assistant (CTA)(m/w/x)
Beschreibung
You will drive medical innovation by managing essential trial documentation and coordinating with cross-functional teams to ensure every clinical study meets strict regulatory standards.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Bachelor's degree in scientific or healthcare-related field
- •Experience or strong interest in clinical research
- •Knowledge of clinical trial processes and regulations
- •Excellent organizational and communication skills
- •Collaborative work style and attention to detail
- •Fluency in German and English
- •Residence in the Hamburg area
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Assist with clinical trial design and analysis
- •Interpret complex medical data
- •Coordinate and administer clinical trials
- •Ensure compliance with protocols and regulatory requirements
- •Maintain and organize clinical trial documentation
- •Manage study files and regulatory submissions
- •Prepare informed consent and case report forms
- •Collaborate with cross-functional teams
- •Track and report clinical trial metrics and milestones
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- •Health insurance offerings
- •Health assessments
Betriebliche Altersvorsorge
- •Competitive retirement planning
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
- zeroPRAXENVollzeit/Teilzeitmit HomeofficeKeine AngabeMannheim
- SGS
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Jobs in der Nähe entdecken
Clinical Trial Assistant (CTA)(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You will drive medical innovation by managing essential trial documentation and coordinating with cross-functional teams to ensure every clinical study meets strict regulatory standards.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Bachelor's degree in scientific or healthcare-related field
- •Experience or strong interest in clinical research
- •Knowledge of clinical trial processes and regulations
- •Excellent organizational and communication skills
- •Collaborative work style and attention to detail
- •Fluency in German and English
- •Residence in the Hamburg area
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Assist with clinical trial design and analysis
- •Interpret complex medical data
- •Coordinate and administer clinical trials
- •Ensure compliance with protocols and regulatory requirements
- •Maintain and organize clinical trial documentation
- •Manage study files and regulatory submissions
- •Prepare informed consent and case report forms
- •Collaborate with cross-functional teams
- •Track and report clinical trial metrics and milestones
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- •Health insurance offerings
- •Health assessments
Betriebliche Altersvorsorge
- •Competitive retirement planning
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 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.
- zeroPRAXEN
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Vollzeitmit HomeofficeQuereinsteigerSpeyer - 176 ICON Clinical Research Germany GmbH
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Vollzeitmit HomeofficeSeniorMannheim - IQVIA
Study Nurse(m/w/x)
Vollzeit/Teilzeitmit HomeofficeJuniorMannheim - doxx GmbH
Sales Assistant / Sales Support(m/w/x)
Vollzeit/TeilzeitBefristeter Vertragmit HomeofficeQuereinsteigerHeidelberg