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Clinical Research Associate 2(m/w/x)
Conducting site visits for clinical trials, supporting subject recruitment plans for medical treatments. Two years of on-site monitoring experience and GCP/ICH knowledge required. Company car, home-office, flexible schedules.
Anforderungen
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Minimum two years of on-site monitoring experience or equivalent combination of education, training and experience
- Knowledge of clinical research regulatory requirements (GCP, ICH guidelines)
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in a fast-paced environment
- Flexibility for business travel (40-60%)
- Driver’s license class B
Aufgaben
- Conduct site selection visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for quality and integrity
- Ensure compliance with GCP and ICH guidelines
- Track regulatory submissions
- Monitor recruitment progress
- Oversee case report form (CRF) completion
- Track data query resolution
- Collaborate with study site experts and client representatives
- Mentor less experienced team members
- Provide subject matter expertise on specific topics
Berufserfahrung
- 2 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Home-Office
- Flexible work schedules
Firmenwagen
- Company car
Sonstige Vorteile
- Accident insurance
Karriere- und Weiterentwicklung
- Career growth resources
Noch nicht perfekt?
- IQVIA RDS GmbHVollzeitRemoteBerufserfahrenFrankfurt am Main
- IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA MedTech
Clinical Research Associate 2(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main
Clinical Research Associate 2(m/w/x)
Conducting site visits for clinical trials, supporting subject recruitment plans for medical treatments. Two years of on-site monitoring experience and GCP/ICH knowledge required. Company car, home-office, flexible schedules.
Anforderungen
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Minimum two years of on-site monitoring experience or equivalent combination of education, training and experience
- Knowledge of clinical research regulatory requirements (GCP, ICH guidelines)
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in a fast-paced environment
- Flexibility for business travel (40-60%)
- Driver’s license class B
Aufgaben
- Conduct site selection visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for quality and integrity
- Ensure compliance with GCP and ICH guidelines
- Track regulatory submissions
- Monitor recruitment progress
- Oversee case report form (CRF) completion
- Track data query resolution
- Collaborate with study site experts and client representatives
- Mentor less experienced team members
- Provide subject matter expertise on specific topics
Berufserfahrung
- 2 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Home-Office
- Flexible work schedules
Firmenwagen
- Company car
Sonstige Vorteile
- Accident insurance
Karriere- und Weiterentwicklung
- Career growth resources
Über das Unternehmen
IQVIA Biotech
Branche
Pharmaceuticals
Beschreibung
The company partners with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas.
Noch nicht perfekt?
- IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA MedTech
Clinical Research Associate 2(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main