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Senior Clinical Research Associate(m/w/x)
Monitoring clinical trial sites, conducting site visits, and training site staff for innovative treatments. Extensive clinical trial monitoring experience and advanced life sciences degree required. Frequent site travel, global team collaboration.
Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Proficiency in relevant clinical trial software and tools
- Excellent communication and interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel at least 60% of the time
- Possession of a valid driver’s license
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
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
Noch nicht perfekt?
- ICON plcVollzeitmit HomeofficeSeniorMannheim
- ICON plc
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Senior Clinical Research Associate(m/w/x)
Monitoring clinical trial sites, conducting site visits, and training site staff for innovative treatments. Extensive clinical trial monitoring experience and advanced life sciences degree required. Frequent site travel, global team collaboration.
Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Proficiency in relevant clinical trial software and tools
- Excellent communication and interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel at least 60% of the time
- Possession of a valid driver’s license
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
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
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.
Noch nicht perfekt?
- ICON plc
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