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Junior Clinical Research Associate(m/w/x)
Coordinating study setup and monitoring for a global clinical research organization. Relevant clinical trial monitoring experience required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Relevant clinical trial monitoring experience
- University degree in medicine or science or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written communication in English
- Excellent verbal communication in English
- Excellent written communication in German
- Excellent verbal communication in German
- Good social skills for timely query handling
- Willingness to travel as required
- Encouraged to apply even if unsure about requirements
Tasks
- Coordinate study setup and monitoring activities
- Complete accurate study status reports
- Maintain study documentation
- Run sponsor-generated queries efficiently
- Ensure study cost efficiency
- Prepare and review study documentation
- Conduct feasibility studies for new proposals
- Develop strong relationships with stakeholders
- Collaborate with clinical investigators and site staff
- Ensure patient safety
- Comply with ICON's procedures and protocols
- Adhere to regulatory requirements
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
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Junior Clinical Research Associate(m/w/x)
Coordinating study setup and monitoring for a global clinical research organization. Relevant clinical trial monitoring experience required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Relevant clinical trial monitoring experience
- University degree in medicine or science or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written communication in English
- Excellent verbal communication in English
- Excellent written communication in German
- Excellent verbal communication in German
- Good social skills for timely query handling
- Willingness to travel as required
- Encouraged to apply even if unsure about requirements
Tasks
- Coordinate study setup and monitoring activities
- Complete accurate study status reports
- Maintain study documentation
- Run sponsor-generated queries efficiently
- Ensure study cost efficiency
- Prepare and review study documentation
- Conduct feasibility studies for new proposals
- Develop strong relationships with stakeholders
- Collaborate with clinical investigators and site staff
- Ensure patient safety
- Comply with ICON's procedures and protocols
- Adhere to regulatory requirements
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- 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 Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Not a perfect match?
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