Die KI-Suchmaschine für Jobs
Senior Clinical Research Associate(m/w/x)
Beschreibung
As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulations while supporting site staff and fostering strong relationships to facilitate successful trial execution.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Advanced degree in a relevant field
- •Extensive experience as a Clinical Research Associate
- •Strong organizational and problem-solving skills
- •Expertise in monitoring practices and data integrity
- •Excellent communication and interpersonal skills
- •Ability to travel at least 60% of the time
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Monitor clinical trial sites for protocol adherence
- •Conduct site visits to assess performance and resolve issues
- •Collaborate with teams for accurate data collection and reporting
- •Provide training and guidance to site staff and CRAs
- •Build and maintain relationships with site personnel and stakeholders
Tools & Technologien
Sprachen
Englisch – 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
- IQVIAVollzeitmit HomeofficeBerufserfahrenBasel
- PPD Switzerland GmbH
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Senior Clinical Research Associate(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulations while supporting site staff and fostering strong relationships to facilitate successful trial execution.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Advanced degree in a relevant field
- •Extensive experience as a Clinical Research Associate
- •Strong organizational and problem-solving skills
- •Expertise in monitoring practices and data integrity
- •Excellent communication and interpersonal skills
- •Ability to travel at least 60% of the time
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Monitor clinical trial sites for protocol adherence
- •Conduct site visits to assess performance and resolve issues
- •Collaborate with teams for accurate data collection and reporting
- •Provide training and guidance to site staff and CRAs
- •Build and maintain relationships with site personnel and stakeholders
Tools & Technologien
Sprachen
Englisch – 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
Über das Unternehmen
ICON plc
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization.
- IQVIA
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