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Senior / Clinical Research Associate(m/w/x)
Performing CRF review, source document verification, and data query resolution for clinical trials at a Contract Research Organization. On-site monitoring experience in Germany and AMG studies required. Flexible work arrangements, mentorship program.
Anforderungen
- Degree in Life Sciences or equivalent
- On-site monitoring experience in Germany
- Experience in Switzerland is a plus
- Monitoring experience in AMG studies
- Experience in specific therapeutic areas
- Proficiency in German and English
- French language skills are an asset
- Advanced proficiency in MS Office
- Ability to plan and multitask
- Communication and problem-solving skills
- Ability to travel and driver’s license
Aufgaben
- Conduct onsite and remote monitoring visits
- Report on all monitoring visit types
- Perform CRF review and source document verification
- Resolve data queries
- Manage site communication and relationships
- Identify potential clinical sites
- Train less experienced research associates
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
Tools & Technologien
- MS Office
- Word
- Excel
- PowerPoint
- Outlook
Benefits
Attraktive Vergütung
- Competitive salary and benefits
Weiterbildungsangebote
- Extensive onboarding program
Mentoring & Coaching
- Mentorship program
Flexibles Arbeiten
- Excellent and flexible working conditions
Lockere Unternehmenskultur
- Team collaboration and independent work
Noch nicht perfekt?
- PPD Germany GmbH & Co KGVollzeitRemoteJuniorMünchen
- IQVIA Biotech
Clinical Research Associate 2(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main, München, Hamburg - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München, Berlin - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Vollzeit/Teilzeitmit HomeofficeSeniorTübingen, München
Senior / Clinical Research Associate(m/w/x)
Performing CRF review, source document verification, and data query resolution for clinical trials at a Contract Research Organization. On-site monitoring experience in Germany and AMG studies required. Flexible work arrangements, mentorship program.
Anforderungen
- Degree in Life Sciences or equivalent
- On-site monitoring experience in Germany
- Experience in Switzerland is a plus
- Monitoring experience in AMG studies
- Experience in specific therapeutic areas
- Proficiency in German and English
- French language skills are an asset
- Advanced proficiency in MS Office
- Ability to plan and multitask
- Communication and problem-solving skills
- Ability to travel and driver’s license
Aufgaben
- Conduct onsite and remote monitoring visits
- Report on all monitoring visit types
- Perform CRF review and source document verification
- Resolve data queries
- Manage site communication and relationships
- Identify potential clinical sites
- Train less experienced research associates
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
Tools & Technologien
- MS Office
- Word
- Excel
- PowerPoint
- Outlook
Benefits
Attraktive Vergütung
- Competitive salary and benefits
Weiterbildungsangebote
- Extensive onboarding program
Mentoring & Coaching
- Mentorship program
Flexibles Arbeiten
- Excellent and flexible working conditions
Lockere Unternehmenskultur
- Team collaboration and independent work
Über das Unternehmen
PSI CRO
Branche
Pharmaceuticals
Beschreibung
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Noch nicht perfekt?
- PPD Germany GmbH & Co KG
CRA II / Sr CRA - FSP Vaccines(m/w/x)
VollzeitRemoteJuniorMünchen - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main, München, Hamburg - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München, Berlin - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Vollzeit/Teilzeitmit HomeofficeSeniorTübingen, München