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Clinical Research Associate or SrCRA(m/w/x)
On-site monitoring of clinical trials for healthcare clients, covering site selection, initiation, and close-out. Two years of on-site clinical monitoring experience, C1 German/English, and good French/Italian required. Flexible work schedules, home-office.
Anforderungen
- University degree in life science or other scientific discipline or apprenticeship in health care field
- Minimum of two years of on-site monitoring experience or equivalent combination of education, training, and experience
- Knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluent verbal and written language skills in German and English (C1 level) plus good verbal demand in French and Italian
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
Aufgaben
- Perform site selection and initiation visits
- Conduct monitoring and close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for quality and regulatory compliance
- Track regulatory submissions and recruitment progress
- Ensure case report form (CRF) completion and resolve data queries
- Collaborate with study site experts and client representatives
- Engage in remote monitoring and study start-up processes as needed
- Mentor less experienced team members and provide subject matter expertise
Berufserfahrung
- 2 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
- Italienisch – Grundkenntnisse
Benefits
Karriere- und Weiterentwicklung
- Resources that promote career growth
Flexibles Arbeiten
- Flexible work schedules
- Home-office
Weiterbildungsangebote
- Programs to build therapeutic knowledge
Startup-Atmosphäre
- Dynamic work environments
Boni & Prämien
- Bonus
Sonstige Vorteile
- Accident insurance
Noch nicht perfekt?
- ICON plcVollzeitRemoteSeniorBasel
- IQVIA
Internship as Clinical Research Associate(m/w/x)
VollzeitPraktikummit HomeofficeBasel - IQVIA
Regulatory and Start Up Specialist(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel - Boehringer Ingelheim
CRM Key Account Manager (Region East)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel - Boehringer Ingelheim Switzerland
CRM Key Account Manager (Region West)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel
Clinical Research Associate or SrCRA(m/w/x)
On-site monitoring of clinical trials for healthcare clients, covering site selection, initiation, and close-out. Two years of on-site clinical monitoring experience, C1 German/English, and good French/Italian required. Flexible work schedules, home-office.
Anforderungen
- University degree in life science or other scientific discipline or apprenticeship in health care field
- Minimum of two years of on-site monitoring experience or equivalent combination of education, training, and experience
- Knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluent verbal and written language skills in German and English (C1 level) plus good verbal demand in French and Italian
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
Aufgaben
- Perform site selection and initiation visits
- Conduct monitoring and close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for quality and regulatory compliance
- Track regulatory submissions and recruitment progress
- Ensure case report form (CRF) completion and resolve data queries
- Collaborate with study site experts and client representatives
- Engage in remote monitoring and study start-up processes as needed
- Mentor less experienced team members and provide subject matter expertise
Berufserfahrung
- 2 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
- Italienisch – Grundkenntnisse
Benefits
Karriere- und Weiterentwicklung
- Resources that promote career growth
Flexibles Arbeiten
- Flexible work schedules
- Home-office
Weiterbildungsangebote
- Programs to build therapeutic knowledge
Startup-Atmosphäre
- Dynamic work environments
Boni & Prämien
- Bonus
Sonstige Vorteile
- Accident insurance
Über das Unternehmen
IQVIA
Branche
Healthcare
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Noch nicht perfekt?
- ICON plc
Senior Clinical Research Associate(m/w/x)
VollzeitRemoteSeniorBasel - IQVIA
Internship as Clinical Research Associate(m/w/x)
VollzeitPraktikummit HomeofficeBasel - IQVIA
Regulatory and Start Up Specialist(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel - Boehringer Ingelheim
CRM Key Account Manager (Region East)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel - Boehringer Ingelheim Switzerland
CRM Key Account Manager (Region West)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBasel