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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
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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