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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
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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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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