ICON plc
Senior Clinical Research Associate(m/w/x)
Full-timeRemoteSenior
Basel
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IQIQVIA
Clinical Research Associate or SrCRA(m/w/x)
Basel
Full-timeWith Home OfficeExperienced
Nejo AI Summary
On-site monitoring of clinical trials for healthcare clients, covering site selection, initiation, and close-out. Two years of on-site clinical monitoring experience, C1 German/English, and good French/Italian required. Flexible work schedules, home-office.
Requirements
- University degree in life science or other scientific discipline or apprenticeship in health care field
- Minimum of two years of on-site monitoring experience or equivalent combination of education, training, and experience
- Knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluent verbal and written language skills in German and English (C1 level) plus good verbal demand in French and Italian
- 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 resolve data queries
- 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 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
- French – Basic
- Italian – Basic
Benefits
Career Advancement
- Resources that promote career growth
Flexible Working
- Flexible work schedules
- Home-office
Learning & Development
- Programs to build therapeutic knowledge
Startup Environment
- Dynamic work environments
Bonuses & Incentives
- Bonus
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.
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IQIQVIA
Clinical Research Associate or SrCRA(m/w/x)
Basel
Full-timeWith Home OfficeExperienced
Nejo AI Summary
On-site monitoring of clinical trials for healthcare clients, covering site selection, initiation, and close-out. Two years of on-site clinical monitoring experience, C1 German/English, and good French/Italian required. Flexible work schedules, home-office.
Requirements
- University degree in life science or other scientific discipline or apprenticeship in health care field
- Minimum of two years of on-site monitoring experience or equivalent combination of education, training, and experience
- Knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluent verbal and written language skills in German and English (C1 level) plus good verbal demand in French and Italian
- 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 resolve data queries
- 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 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
- French – Basic
- Italian – Basic
Benefits
Career Advancement
- Resources that promote career growth
Flexible Working
- Flexible work schedules
- Home-office
Learning & Development
- Programs to build therapeutic knowledge
Startup Environment
- Dynamic work environments
Bonuses & Incentives
- Bonus
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.
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