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Clinical Research Associate 1 or 2 Single Sponsor(m/w/x)
On-site monitoring and close-out visits for clinical trials at a global CRO. Subject recruitment planning and GCP compliance evaluation required. Home-office, company car, and flexible schedules.
Requirements
- University degree in life science or scientific discipline, or healthcare apprenticeship
- Minimum 12 months on-site monitoring experience
- Knowledge of GCP and ICH guidelines
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in fast-paced environment
- German fluency at C1 level
- Good command of English
- Flexibility for travel up to 40-60%
- Driver's license class B
Tasks
- Conduct site selection, initiation, monitoring, and close-out visits
- Develop a subject recruitment plan
- Evaluate site practices for compliance with GCP and ICH guidelines
- Track regulatory submissions, recruitment, CRF completion, and data query resolution
- Collaborate with study site experts and client representatives
- Participate in remote monitoring and study start-up processes
- Specialize in therapeutic areas, including pharmaceutical products or medical devices
- Mentor less experienced team members
- Provide expertise on specific topics or additional tasks
Work Experience
- 1 year
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Flexible Working
- Home-office
- Flexible working schedules
Company Vehicle
- Company car or car allowance
Other Benefits
- Accident insurance
Retirement Plans
- Pension
Career Advancement
- Career growth resources
Startup Environment
- Dynamic work environments
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Clinical Research Associate 1 or 2 Single Sponsor(m/w/x)
On-site monitoring and close-out visits for clinical trials at a global CRO. Subject recruitment planning and GCP compliance evaluation required. Home-office, company car, and flexible schedules.
Requirements
- University degree in life science or scientific discipline, or healthcare apprenticeship
- Minimum 12 months on-site monitoring experience
- Knowledge of GCP and ICH guidelines
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in fast-paced environment
- German fluency at C1 level
- Good command of English
- Flexibility for travel up to 40-60%
- Driver's license class B
Tasks
- Conduct site selection, initiation, monitoring, and close-out visits
- Develop a subject recruitment plan
- Evaluate site practices for compliance with GCP and ICH guidelines
- Track regulatory submissions, recruitment, CRF completion, and data query resolution
- Collaborate with study site experts and client representatives
- Participate in remote monitoring and study start-up processes
- Specialize in therapeutic areas, including pharmaceutical products or medical devices
- Mentor less experienced team members
- Provide expertise on specific topics or additional tasks
Work Experience
- 1 year
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Flexible Working
- Home-office
- Flexible working schedules
Company Vehicle
- Company car or car allowance
Other Benefits
- Accident insurance
Retirement Plans
- Pension
Career Advancement
- Career growth resources
Startup Environment
- Dynamic work environments
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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