IQVIA
Clinical Research Associate or SrCRA(m/w/x)
Full-timeWith HomeofficeExperienced
Basel
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ICICON plc
Senior Clinical Research Associate(m/w/x)
Basel
Full-timeRemoteSenior
Nejo AI Summary
Monitoring clinical trial sites for protocol adherence and data integrity at a global clinical research organization. Extensive experience in clinical trial monitoring and site management required. International site visits.
Requirements
- Advanced degree in a relevant field
- Extensive experience as a Clinical Research Associate
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Excellent communication and interpersonal skills
- Ability to travel at least 60% of the time
Tasks
- Monitor clinical trial sites for protocol adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with teams for accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain relationships with site personnel and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial software
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Flexible optional benefits
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc 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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ICICON plc
Senior Clinical Research Associate(m/w/x)
Basel
Full-timeRemoteSenior
Nejo AI Summary
Monitoring clinical trial sites for protocol adherence and data integrity at a global clinical research organization. Extensive experience in clinical trial monitoring and site management required. International site visits.
Requirements
- Advanced degree in a relevant field
- Extensive experience as a Clinical Research Associate
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Excellent communication and interpersonal skills
- Ability to travel at least 60% of the time
Tasks
- Monitor clinical trial sites for protocol adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with teams for accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain relationships with site personnel and stakeholders
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- clinical trial software
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Flexible optional benefits
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc 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
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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