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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
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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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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