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Clinical Research Associate 2 / CRA 2(m/w/x)
Site selection, initiation, and monitoring visits for clinical trials in life sciences. 2-4 years on-site clinical monitoring experience required. Company car provided.
Requirements
- University degree in life science, other scientific discipline, or apprenticeship in health care
- Minimum two to four years of on-site monitoring experience or equivalent combination of education, training, and 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
- Monitor case report form completion and data queries
- Collaborate with study site experts and client representatives
- Engage in remote monitoring and 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
- 2 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Career Advancement
- Career growth resources
Not a perfect match?
- IQVIAFull-timeWith HomeofficeSeniorFrankfurt am Main
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Clinical Research Associate 2 / CRA 2(m/w/x)
Site selection, initiation, and monitoring visits for clinical trials in life sciences. 2-4 years on-site clinical monitoring experience required. Company car provided.
Requirements
- University degree in life science, other scientific discipline, or apprenticeship in health care
- Minimum two to four years of on-site monitoring experience or equivalent combination of education, training, and 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
- Monitor case report form completion and data queries
- Collaborate with study site experts and client representatives
- Engage in remote monitoring and 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
- 2 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Career Advancement
- Career growth resources
About the Company
IQVIA RDS GmbH
Industry
Healthcare
Description
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
Not a perfect match?
- IQVIA
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