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Clinical Trial Assistant (CTA)(m/w/x)
Assisting with clinical trial design and analysis, interpreting complex medical data at a global clinical research organization. Bachelor's degree in scientific or healthcare field required. Global Employee Assistance Programme.
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
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
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
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
Noch nicht perfekt?
- ICON plcVollzeitmit HomeofficeJuniorMannheim
- ICON plc
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Administrative Assistant im Bereich Legal & Compliance(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim
Clinical Trial Assistant (CTA)(m/w/x)
Assisting with clinical trial design and analysis, interpreting complex medical data at a global clinical research organization. Bachelor's degree in scientific or healthcare field required. Global Employee Assistance Programme.
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
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
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
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.
Noch nicht perfekt?
- ICON plc
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VollzeitRemoteSeniorMannheim - SGS
Chemielaborant:in / CTA / Quereinsteiger:in(m/w/x)
Vollzeitmit HomeofficeQuereinsteigerSpeyer - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorMannheim - knoell
Administrative Assistant im Bereich Legal & Compliance(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim