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Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
Protocol adherence monitoring at clinical trial sites, including site visits and staff training. Advanced life sciences degree and multi-site project management ability required. Global Employee Assistance Programme, with extensive site travel.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication and interpersonal skills
- Fluency in German and English
- 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
- German – Business Fluent
- English – Business Fluent
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
Not a perfect match?
- ICON plcFull-timeWith HomeofficeSeniorFrankfurt am Main
- ICON plc
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
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(Senior) Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Full-timeRemoteNot specifiedFrankfurt am Main - ICON plc
Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main
Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
Protocol adherence monitoring at clinical trial sites, including site visits and staff training. Advanced life sciences degree and multi-site project management ability required. Global Employee Assistance Programme, with extensive site travel.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication and interpersonal skills
- Fluency in German and English
- 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
- German – Business Fluent
- English – Business Fluent
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
About the Company
176 ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovative treatments.
Not a perfect match?
- ICON plc
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