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Senior Clinical Research Associate - Ofthalmology area(m/w/x)
On-site monitoring of ophthalmology clinical trials for protocol adherence and GCP compliance. Extensive experience as a CRA and advanced degree in life sciences or medicine required. Global employee assistance program, life assurance, and retirement planning offerings.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring and data integrity
- Proficiency in clinical trial software
- Excellent communication and stakeholder management skills
- Fluency in English and German
- Ability to travel 60% of time
- Valid driver’s license
- Ophthalmology experience
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure regulatory and GCP standard compliance
- Conduct site visits to assess performance
- Resolve site issues and provide execution support
- Collaborate with cross-functional teams for data collection
- Ensure timely and accurate data reporting
- Train and guide site staff and CRAs
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
- Liaise with stakeholders to facilitate trial operations
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- clinical trial software
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
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Senior Clinical Research Associate - Ofthalmology area(m/w/x)
On-site monitoring of ophthalmology clinical trials for protocol adherence and GCP compliance. Extensive experience as a CRA and advanced degree in life sciences or medicine required. Global employee assistance program, life assurance, and retirement planning offerings.
Requirements
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring and data integrity
- Proficiency in clinical trial software
- Excellent communication and stakeholder management skills
- Fluency in English and German
- Ability to travel 60% of time
- Valid driver’s license
- Ophthalmology experience
Tasks
- Monitor clinical trial sites for protocol adherence
- Ensure regulatory and GCP standard compliance
- Conduct site visits to assess performance
- Resolve site issues and provide execution support
- Collaborate with cross-functional teams for data collection
- Ensure timely and accurate data reporting
- Train and guide site staff and CRAs
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
- Liaise with stakeholders to facilitate trial operations
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- clinical trial software
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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