Dein persönlicher KI-Karriere-Agent
Senior Clinical Trial Manager(m/w/x)
Developing monitoring plans and training CRAs for innovative treatment studies. Subject matter expertise in a therapeutic area required. Up to 20% travel expected.
Anforderungen
- 4 year degree or equivalent combination of education & experience
- Demonstrated ability to drive clinical deliverables of a study
- Subject matter expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
- Fluency in local language - both written & verbal
Aufgaben
- Oversee the clinical budget
- Develop monitoring plans and tools
- Train Clinical Research Associates (CRAs)
- Drive enrollment and study start-up activities
- Review trip reports
- Implement corrective and preventative action plans
- Liaise with the Sponsor, vendors, and cross-functional teams
- Identify and mitigate risks impacting clinical delivery
- Provide reporting and metrics on clinical activities
- Participate in Sponsor, Investigator, and bid defense meetings
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- local – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Sonstige Zulagen
- Flexible optional benefits
Gefällt dir diese Stelle?
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Senior Clinical Trial Manager(m/w/x)
Developing monitoring plans and training CRAs for innovative treatment studies. Subject matter expertise in a therapeutic area required. Up to 20% travel expected.
Anforderungen
- 4 year degree or equivalent combination of education & experience
- Demonstrated ability to drive clinical deliverables of a study
- Subject matter expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
- Fluency in local language - both written & verbal
Aufgaben
- Oversee the clinical budget
- Develop monitoring plans and tools
- Train Clinical Research Associates (CRAs)
- Drive enrollment and study start-up activities
- Review trip reports
- Implement corrective and preventative action plans
- Liaise with the Sponsor, vendors, and cross-functional teams
- Identify and mitigate risks impacting clinical delivery
- Provide reporting and metrics on clinical activities
- Participate in Sponsor, Investigator, and bid defense meetings
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- local – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Sonstige Zulagen
- 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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