IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperienced
Frankfurt am Main
New Job?Nejo!
The AI Job Search Engine
IQIQVIA MedTech
Clinical Research Associate 2(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Monitoring medical device trials for a global life sciences provider, including site selection and close-out visits. Two years on-site monitoring experience and ISO 14155 knowledge required. Company car, home-office, flexible schedules.
Requirements
- Degree in life science, scientific discipline, or healthcare apprenticeship
- Two years on-site monitoring experience or equivalent combination
- Preferred experience in medical devices trials
- Knowledge of GCP and ICH guidelines
- In depth knowledge of ISO 14155
- Strong communication skills and attention to detail
- Fluency in German and good English command
- Flexibility for business travel up to 50%
- Strong IT skills and Microsoft Office proficiency
- Preferable driver’s license class B
Tasks
- Perform site selection and initiation visits
- Conduct monitoring and close-out visits
- Monitor medical device clinical trials
- Support subject recruitment plan development
- Evaluate site practice quality and integrity
- Ensure compliance with GCP and ISO 14155
- Track regulatory submissions and recruitment progress
- Manage CRF completion and data queries
- Collaborate with site experts and clients
- Mentor less experienced team members
- Act as a subject matter expert
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- GCP
- ICH guidelines
- ISO 14155
- Microsoft Office
- Word
- Excel
- PowerPoint
Benefits
Flexible Working
- Home-Office
- Flexible work schedules
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Career Advancement
- Career growth resources
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA MedTech 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
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main, München, Hamburg
IQIQVIA MedTech
Clinical Research Associate 2(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Monitoring medical device trials for a global life sciences provider, including site selection and close-out visits. Two years on-site monitoring experience and ISO 14155 knowledge required. Company car, home-office, flexible schedules.
Requirements
- Degree in life science, scientific discipline, or healthcare apprenticeship
- Two years on-site monitoring experience or equivalent combination
- Preferred experience in medical devices trials
- Knowledge of GCP and ICH guidelines
- In depth knowledge of ISO 14155
- Strong communication skills and attention to detail
- Fluency in German and good English command
- Flexibility for business travel up to 50%
- Strong IT skills and Microsoft Office proficiency
- Preferable driver’s license class B
Tasks
- Perform site selection and initiation visits
- Conduct monitoring and close-out visits
- Monitor medical device clinical trials
- Support subject recruitment plan development
- Evaluate site practice quality and integrity
- Ensure compliance with GCP and ISO 14155
- Track regulatory submissions and recruitment progress
- Manage CRF completion and data queries
- Collaborate with site experts and clients
- Mentor less experienced team members
- Act as a subject matter expert
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- GCP
- ICH guidelines
- ISO 14155
- Microsoft Office
- Word
- Excel
- PowerPoint
Benefits
Flexible Working
- Home-Office
- Flexible work schedules
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Career Advancement
- Career growth resources
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA MedTech 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 MedTech
Industry
Healthcare
Description
IQVIA is a global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries, accelerating the development of innovative medical treatments.
Not a perfect match?
- IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main, München, Hamburg