Dein persönlicher KI-Karriere-Agent
CRA II/ Senior CRA(m/w/x)
Overseeing clinical trial sites from qualification to close-out for new drug development at a global CRO. 2+ years of clinical research monitoring experience and in-depth ICH-GCP knowledge required. Frequent site visits for diverse clinical studies.
Anforderungen
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Excellent communication skills in German and English
Aufgaben
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial progress
- Perform close-out visits for trials
- Ensure protocol compliance
- Maintain data integrity
- Prioritize patient safety during trials
- Collaborate with investigators and site staff
- Facilitate smooth study conduct
- Review and resolve data queries
- Prepare and review study documentation
- Draft clinical study reports
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
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CRA II/ Senior CRA(m/w/x)
Overseeing clinical trial sites from qualification to close-out for new drug development at a global CRO. 2+ years of clinical research monitoring experience and in-depth ICH-GCP knowledge required. Frequent site visits for diverse clinical studies.
Anforderungen
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Excellent communication skills in German and English
Aufgaben
- Conduct site qualification visits
- Initiate clinical trial sites
- Monitor clinical trial progress
- Perform close-out visits for trials
- Ensure protocol compliance
- Maintain data integrity
- Prioritize patient safety during trials
- Collaborate with investigators and site staff
- Facilitate smooth study conduct
- Review and resolve data queries
- Prepare and review study documentation
- Draft clinical study reports
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
176 ICON Clinical Research Germany GmbH
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovative treatments.
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