The AI Job Search Engine
Clinical Research Associate I or II(m/w/x)
Site selection, monitoring, and close-out visits for clinical trials at a human data science firm. One year on-site monitoring experience and C1 German fluency essential. Flexible work schedules, home-office option.
Requirements
- University degree in life science, other scientific discipline, or apprenticeship in health care
- Minimum of one year of on-site monitoring experience
- Knowledge of clinical research regulatory requirements, GCP, and ICH guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluency in German at C1 level and good command of English
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
Tasks
- 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 integrity
- Ensure compliance with GCP and ICH guidelines
- Track regulatory submissions and recruitment progress
- Manage case report form (CRF) completion
- Resolve data queries
- Collaborate with study site experts and client representatives
- Participate in remote monitoring as needed
- Engage in study start-up processes
- Specialize in therapeutic areas for pharmaceutical products or medical devices
- Mentor less experienced team members
- Act as a subject matter expert for specific topics
Work Experience
- 1 year
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Career Advancement
- Resources that promote career growth
Flexible Working
- Support for flexible work schedules
- Home-office
Learning & Development
- Programs to build therapeutic knowledge
Startup Environment
- Dynamic work environments
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Not a perfect match?
- IQVIAFull-timeWith HomeofficeSeniorWienfrom 4,200 / month
- IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 4,000 / month - IQVIA Biotech
Clinical Associate Regulatory Submissions(m/w/x)
Full-timeWith HomeofficeJuniorWien - ICON plc
Sr. Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeExperiencedWien - PSI CRO
Site Identification Specialist(m/w/x)
Full-timeWith HomeofficeJuniorWienfrom 70,000 / year
Clinical Research Associate I or II(m/w/x)
Site selection, monitoring, and close-out visits for clinical trials at a human data science firm. One year on-site monitoring experience and C1 German fluency essential. Flexible work schedules, home-office option.
Requirements
- University degree in life science, other scientific discipline, or apprenticeship in health care
- Minimum of one year of on-site monitoring experience
- Knowledge of clinical research regulatory requirements, GCP, and ICH guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluency in German at C1 level and good command of English
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
Tasks
- 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 integrity
- Ensure compliance with GCP and ICH guidelines
- Track regulatory submissions and recruitment progress
- Manage case report form (CRF) completion
- Resolve data queries
- Collaborate with study site experts and client representatives
- Participate in remote monitoring as needed
- Engage in study start-up processes
- Specialize in therapeutic areas for pharmaceutical products or medical devices
- Mentor less experienced team members
- Act as a subject matter expert for specific topics
Work Experience
- 1 year
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Career Advancement
- Resources that promote career growth
Flexible Working
- Support for flexible work schedules
- Home-office
Learning & Development
- Programs to build therapeutic knowledge
Startup Environment
- Dynamic work environments
Company Vehicle
- Company car
Other Benefits
- Accident insurance
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Not a perfect match?
- IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 4,200 / month - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeWith HomeofficeExperiencedWienfrom 4,000 / month - IQVIA Biotech
Clinical Associate Regulatory Submissions(m/w/x)
Full-timeWith HomeofficeJuniorWien - ICON plc
Sr. Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeExperiencedWien - PSI CRO
Site Identification Specialist(m/w/x)
Full-timeWith HomeofficeJuniorWienfrom 70,000 / year