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Clinical Research Associate 2(m/w/x)
On-site monitoring for clinical development across all phases at biotech and biopharma partners. Two years on-site monitoring experience and German fluency required. Company car for private use.
Requirements
- Degree in life science, scientific discipline, or healthcare apprenticeship
- Two years on-site monitoring experience or equivalent combination
- Knowledge of GCP and ICH guidelines
- Strong communication, attention to detail, and pace-resilience
- Fluency in German and good English command
- Flexibility for business travel up to 60%
- Driver’s license class B
Tasks
- Perform site selection, initiation, monitoring, and close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for GCP and ICH compliance
- Track regulatory submissions and recruitment progress
- Manage CRF completion and data query resolution
- Collaborate with study site experts and client representatives
- Mentor less experienced team members
- Act as a subject matter expert for specific topics
Work Experience
- 2 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
Benefits
Job Security
- Permanent contract
Flexible Working
- Home-Office
- Flexible work schedules
Career Advancement
- Career growth resources
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Not a perfect match?
- IQVIAFull-timeWith HomeofficeSeniorWienfrom 4,200 / month
- IQVIA
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Sr. Clinical Research Associate(m/w/x)
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Senior Clinical Research Associate(m/w/x)
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Clinical Research Associate 2(m/w/x)
On-site monitoring for clinical development across all phases at biotech and biopharma partners. Two years on-site monitoring experience and German fluency required. Company car for private use.
Requirements
- Degree in life science, scientific discipline, or healthcare apprenticeship
- Two years on-site monitoring experience or equivalent combination
- Knowledge of GCP and ICH guidelines
- Strong communication, attention to detail, and pace-resilience
- Fluency in German and good English command
- Flexibility for business travel up to 60%
- Driver’s license class B
Tasks
- Perform site selection, initiation, monitoring, and close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for GCP and ICH compliance
- Track regulatory submissions and recruitment progress
- Manage CRF completion and data query resolution
- Collaborate with study site experts and client representatives
- Mentor less experienced team members
- Act as a subject matter expert for specific topics
Work Experience
- 2 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
Benefits
Job Security
- Permanent contract
Flexible Working
- Home-Office
- Flexible work schedules
Career Advancement
- Career growth resources
Company Vehicle
- Company car
Other Benefits
- Accident insurance
About the Company
IQVIA Biotech
Industry
Pharmaceuticals
Description
The company partners with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas.
Not a perfect match?
- IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
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Sr. Clinical Research Associate(m/w/x)
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Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorWien - IQVIA Biotech
Clinical Associate Regulatory Submissions(m/w/x)
Full-timeWith HomeofficeJuniorWien