IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
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IQIQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeExperienced
Nejo AI Summary
On-site monitoring and evaluation of clinical trial practices for multiple sponsors. Two years of on-site clinical monitoring experience required. Flexible work schedules, home-office option.
Requirements
- University degree in life science, scientific discipline, or apprenticeship in health care
- Minimum of two years of on-site monitoring 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
- Good command of German and English
- Flexibility for business travel up to 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
- Complete case report forms and resolve data queries
- Collaborate with study site experts and client representatives
Work Experience
- 2 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/car allowance
Other Benefits
- Accident insurance
Retirement Plans
- Pension
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA RDS GmbH 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?
- IQVIA RDS GmbH
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Clinical Research Associate - Sponsor dedicated(m/w/x)
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Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA
Clinical Research Associate 1 or 2, Single Sponsor(m/w/x)
Full-timeRemoteJuniorFrankfurt am Main
IQIQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeExperienced
Nejo AI Summary
On-site monitoring and evaluation of clinical trial practices for multiple sponsors. Two years of on-site clinical monitoring experience required. Flexible work schedules, home-office option.
Requirements
- University degree in life science, scientific discipline, or apprenticeship in health care
- Minimum of two years of on-site monitoring 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
- Good command of German and English
- Flexibility for business travel up to 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
- Complete case report forms and resolve data queries
- Collaborate with study site experts and client representatives
Work Experience
- 2 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/car allowance
Other Benefits
- Accident insurance
Retirement Plans
- Pension
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA RDS GmbH 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 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
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA
Clinical Research Associate 1 or 2, Single Sponsor(m/w/x)
Full-timeRemoteJuniorFrankfurt am Main