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Developing monitoring plans and tools for global clinical trials at a clinical research organization. 10+ years clinical trial management experience required. Global Employee Assistance Programme, family well-being support.
Requirements
- Minimum 4+ years experience in Clinical Trial Management at CRO or Pharmaceutical Organization
- Bachelor's degree in health, life sciences, or relevant fields
- Minimum 10+ years relevant experience in clinical trial management
- Preferred: 2+ years monitoring experience
- Advantageous: Experience managing complex or global trials
- Preferred: Experience managing all trial components (start-up to database lock)
- Preferred: Experience coaching/mentoring CTMs, leading CTM teams, and participating in departmental initiatives
- Fluency in English (reading, writing, speaking)
Tasks
- Oversee the clinical budget
- Ensure efficient resource allocation
- Develop monitoring plans and tools
- Ensure effective study oversight
- Train Clinical Research Associates (CRAs)
- Mentor Clinical Research Associates (CRAs)
- Drive study enrollment
- Lead study start-up activities
- Adhere to study timelines
- Review trip reports
- Implement corrective action plans
- Implement preventative action plans
- Foster relationships with Sponsors
- Foster relationships with vendors
- Foster relationships with cross-functional teams
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Family Support
- Family well-being support
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Not a perfect match?
- 176 ICON Clinical Research Germany GmbHFull-timeWith HomeofficeSeniorMannheim
- ICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - 176 ICON Clinical Research Germany GmbH
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Study Start Up Associate(m/w/x)
Full-timeWith HomeofficeJuniorMannheim - ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Full-timeWith HomeofficeExperiencedMannheim
Developing monitoring plans and tools for global clinical trials at a clinical research organization. 10+ years clinical trial management experience required. Global Employee Assistance Programme, family well-being support.
Requirements
- Minimum 4+ years experience in Clinical Trial Management at CRO or Pharmaceutical Organization
- Bachelor's degree in health, life sciences, or relevant fields
- Minimum 10+ years relevant experience in clinical trial management
- Preferred: 2+ years monitoring experience
- Advantageous: Experience managing complex or global trials
- Preferred: Experience managing all trial components (start-up to database lock)
- Preferred: Experience coaching/mentoring CTMs, leading CTM teams, and participating in departmental initiatives
- Fluency in English (reading, writing, speaking)
Tasks
- Oversee the clinical budget
- Ensure efficient resource allocation
- Develop monitoring plans and tools
- Ensure effective study oversight
- Train Clinical Research Associates (CRAs)
- Mentor Clinical Research Associates (CRAs)
- Drive study enrollment
- Lead study start-up activities
- Adhere to study timelines
- Review trip reports
- Implement corrective action plans
- Implement preventative action plans
- Foster relationships with Sponsors
- Foster relationships with vendors
- Foster relationships with cross-functional teams
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Competitive retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Family Support
- Family well-being support
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - 176 ICON Clinical Research Germany GmbH
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Study Start Up Associate(m/w/x)
Full-timeWith HomeofficeJuniorMannheim - ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Full-timeWith HomeofficeExperiencedMannheim