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Early Development Clinical Research Associate II(m/w/x)
On-site monitoring and close-out visits for early-phase oncology trials. 2+ years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, company car for private use.
Requirements
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills
- Attention to detail
- Ability to work independently
- Ability to work collaboratively
- Ability to work in fast-paced environment
- Ability to travel at least 60% of time
- International and domestic travel
- Valid driver's license
- Encouraged to apply even if not meeting all requirements
Tasks
- Conduct site qualification visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Ensure protocol compliance
- Ensure data integrity
- Ensure patient safety
- Collaborate with investigators
- Collaborate with site staff
- Perform data review
- Resolve data queries
- Contribute to study documentation preparation
- Contribute to study documentation review
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
Mental Health Support
- 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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Early Development Clinical Research Associate II(m/w/x)
On-site monitoring and close-out visits for early-phase oncology trials. 2+ years CRA experience with ICH-GCP knowledge required. 4 weeks vacation, company car for private use.
Requirements
- Bachelor's degree in scientific or healthcare field
- Minimum 2 years as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, ICH-GCP
- Strong organizational and communication skills
- Attention to detail
- Ability to work independently
- Ability to work collaboratively
- Ability to work in fast-paced environment
- Ability to travel at least 60% of time
- International and domestic travel
- Valid driver's license
- Encouraged to apply even if not meeting all requirements
Tasks
- Conduct site qualification visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Ensure protocol compliance
- Ensure data integrity
- Ensure patient safety
- Collaborate with investigators
- Collaborate with site staff
- Perform data review
- Resolve data queries
- Contribute to study documentation preparation
- Contribute to study documentation review
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
Mental Health Support
- 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
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- ICON plc
Clinical Research Associate II(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main, München, Hamburg - ICON plc
Clinical Research Associate - Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main