Dein persönlicher KI-Karriere-Agent
Early Development Clinical Research Associate II(m/w/x)
On-site monitoring and close-out visits for early-phase oncology trials. 2+ years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, company car for private use.
Anforderungen
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills
- Attention to detail
- Ability to work independently
- Ability to work collaboratively
- Ability to work in fast-paced environment
- Ability to travel at least 60% of time
- International and domestic travel
- Valid driver's license
- Encouraged to apply even if not meeting all requirements
Aufgaben
- Conduct site qualification visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Ensure protocol compliance
- Ensure data integrity
- Ensure patient safety
- Collaborate with investigators
- Collaborate with site staff
- Perform data review
- Resolve data queries
- Contribute to study documentation preparation
- Contribute to study documentation review
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning
Mentale Gesundheitsförderung
- Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
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Early Development Clinical Research Associate II(m/w/x)
On-site monitoring and close-out visits for early-phase oncology trials. 2+ years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, company car for private use.
Anforderungen
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills
- Attention to detail
- Ability to work independently
- Ability to work collaboratively
- Ability to work in fast-paced environment
- Ability to travel at least 60% of time
- International and domestic travel
- Valid driver's license
- Encouraged to apply even if not meeting all requirements
Aufgaben
- Conduct site qualification visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Ensure protocol compliance
- Ensure data integrity
- Ensure patient safety
- Collaborate with investigators
- Collaborate with site staff
- Perform data review
- Resolve data queries
- Contribute to study documentation preparation
- Contribute to study documentation review
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning
Mentale Gesundheitsförderung
- 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 plc
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Noch nicht perfekt?
- ICON plc
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