IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperienced
Frankfurt am Main
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IQIQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Conducting site selection, monitoring, and close-out visits for clinical trials at a human data science company. German C1 fluency essential. Flexible work schedules, home-office option.
Requirements
- University degree in life science or other scientific discipline or apprenticeship in health care field
- Minimum of two to four years of on-site monitoring experience or equivalent combination of education, training, and experience
- Knowledge of clinical research regulatory requirements, i.e., 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 regulatory compliance
- Track regulatory submissions and recruitment progress
- Ensure case report form (CRF) completion and data query resolution
- Collaborate with study site experts and client representatives
- Engage in remote monitoring and study start-up processes as needed
- Mentor less experienced team members and provide subject matter expertise
Work Experience
- 2 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Career Advancement
- Career growth resources
Flexible Working
- Flexible work schedules
- Home-office
Mental Health Support
- Therapeutic knowledge programs
Startup Environment
- Dynamic work environments
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Clinical Research Associate 1 or 2, Single Sponsor(m/w/x)
Full-timeRemoteJuniorFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main
IQIQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Conducting site selection, monitoring, and close-out visits for clinical trials at a human data science company. German C1 fluency essential. Flexible work schedules, home-office option.
Requirements
- University degree in life science or other scientific discipline or apprenticeship in health care field
- Minimum of two to four years of on-site monitoring experience or equivalent combination of education, training, and experience
- Knowledge of clinical research regulatory requirements, i.e., 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 regulatory compliance
- Track regulatory submissions and recruitment progress
- Ensure case report form (CRF) completion and data query resolution
- Collaborate with study site experts and client representatives
- Engage in remote monitoring and study start-up processes as needed
- Mentor less experienced team members and provide subject matter expertise
Work Experience
- 2 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Career Advancement
- Career growth resources
Flexible Working
- Flexible work schedules
- Home-office
Mental Health Support
- Therapeutic knowledge programs
Startup Environment
- Dynamic work environments
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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 RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Clinical Research Associate 1 or 2, Single Sponsor(m/w/x)
Full-timeRemoteJuniorFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main