Dein persönlicher KI-Karriere-Agent
Junior Clinical Research Associate(m/w/x)
Coordinating study setup and monitoring for a global clinical research organization. Relevant clinical trial monitoring experience required. Annual leave entitlements, health insurance, and retirement planning.
Anforderungen
- Relevant clinical trial monitoring experience
- University degree in medicine or science or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written communication in English
- Excellent verbal communication in English
- Excellent written communication in German
- Excellent verbal communication in German
- Good social skills for timely query handling
- Willingness to travel as required
- Encouraged to apply even if unsure about requirements
Aufgaben
- Coordinate study setup and monitoring activities
- Complete accurate study status reports
- Maintain study documentation
- Run sponsor-generated queries efficiently
- Ensure study cost efficiency
- Prepare and review study documentation
- Conduct feasibility studies for new proposals
- Develop strong relationships with stakeholders
- Collaborate with clinical investigators and site staff
- Ensure patient safety
- Comply with ICON's procedures and protocols
- Adhere to regulatory requirements
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – 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.
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Junior Clinical Research Associate(m/w/x)
Coordinating study setup and monitoring for a global clinical research organization. Relevant clinical trial monitoring experience required. Annual leave entitlements, health insurance, and retirement planning.
Anforderungen
- Relevant clinical trial monitoring experience
- University degree in medicine or science or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written communication in English
- Excellent verbal communication in English
- Excellent written communication in German
- Excellent verbal communication in German
- Good social skills for timely query handling
- Willingness to travel as required
- Encouraged to apply even if unsure about requirements
Aufgaben
- Coordinate study setup and monitoring activities
- Complete accurate study status reports
- Maintain study documentation
- Run sponsor-generated queries efficiently
- Ensure study cost efficiency
- Prepare and review study documentation
- Conduct feasibility studies for new proposals
- Develop strong relationships with stakeholders
- Collaborate with clinical investigators and site staff
- Ensure patient safety
- Comply with ICON's procedures and protocols
- Adhere to regulatory requirements
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – 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.
Noch nicht perfekt?
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Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
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Vollzeitnur vor OrtJuniorFrankfurt am Main