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Senior Clinical Trial Manager(m/w/x)
Developing monitoring plans and training CRAs for innovative treatment studies. Subject matter expertise in a therapeutic area required. Up to 20% travel expected.
Requirements
- 4 year degree or equivalent combination of education & experience
- Demonstrated ability to drive clinical deliverables of a study
- Subject matter expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
- Fluency in local language - both written & verbal
Tasks
- Oversee the clinical budget
- Develop monitoring plans and tools
- Train Clinical Research Associates (CRAs)
- Drive enrollment and study start-up activities
- Review trip reports
- Implement corrective and preventative action plans
- Liaise with the Sponsor, vendors, and cross-functional teams
- Identify and mitigate risks impacting clinical delivery
- Provide reporting and metrics on clinical activities
- Participate in Sponsor, Investigator, and bid defense meetings
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- local – 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 Trial Manager(m/w/x)
Developing monitoring plans and training CRAs for innovative treatment studies. Subject matter expertise in a therapeutic area required. Up to 20% travel expected.
Requirements
- 4 year degree or equivalent combination of education & experience
- Demonstrated ability to drive clinical deliverables of a study
- Subject matter expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
- Fluency in local language - both written & verbal
Tasks
- Oversee the clinical budget
- Develop monitoring plans and tools
- Train Clinical Research Associates (CRAs)
- Drive enrollment and study start-up activities
- Review trip reports
- Implement corrective and preventative action plans
- Liaise with the Sponsor, vendors, and cross-functional teams
- Identify and mitigate risks impacting clinical delivery
- Provide reporting and metrics on clinical activities
- Participate in Sponsor, Investigator, and bid defense meetings
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- local – 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.
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