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Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Managing clinical study sites from selection to close-out for medical treatment development. University degree in life science and two years on-site monitoring experience required. Home office, flexible schedules, therapeutic knowledge programs.
Requirements
- University Degree in life science or other scientific discipline or apprenticeship in health care
- Minimum two years on-site monitoring experience
- Knowledge of GCP and ICH guidelines
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in fast-paced environment
- German fluency (C1 level)
- Good command of English
- Flexibility for 40-60% travel
- Driver’s license class B
Tasks
- Conduct site selection visits.
- Initiate study sites.
- Monitor study sites.
- Close out study sites.
- Assist in developing subject recruitment plans.
- Evaluate site practices against GCP and ICH guidelines.
- Track regulatory submissions.
- Track subject recruitment.
- Track CRF completion.
- Track data query resolution.
- Collaborate with study site experts and client representatives.
- Conduct remote monitoring.
- Participate in study start-up processes.
- Specialize in a therapeutic area.
- Mentor less experienced team members.
- Provide subject matter expertise.
- Complete additional assigned tasks.
Work Experience
- 2 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Career Advancement
- Career growth resources
Flexible Working
- Flexible work schedules
- Home office
Mental Health Support
- Therapeutic knowledge programs
Startup Environment
- Dynamic work environments
Company Vehicle
- Company car
Other Benefits
- Accident insurance
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Clinical Site Management Lead(m/w/x)
Full-timeWith HomeofficeSeniorWienfrom 45,080 / year
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Managing clinical study sites from selection to close-out for medical treatment development. University degree in life science and two years on-site monitoring experience required. Home office, flexible schedules, therapeutic knowledge programs.
Requirements
- University Degree in life science or other scientific discipline or apprenticeship in health care
- Minimum two years on-site monitoring experience
- Knowledge of GCP and ICH guidelines
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in fast-paced environment
- German fluency (C1 level)
- Good command of English
- Flexibility for 40-60% travel
- Driver’s license class B
Tasks
- Conduct site selection visits.
- Initiate study sites.
- Monitor study sites.
- Close out study sites.
- Assist in developing subject recruitment plans.
- Evaluate site practices against GCP and ICH guidelines.
- Track regulatory submissions.
- Track subject recruitment.
- Track CRF completion.
- Track data query resolution.
- Collaborate with study site experts and client representatives.
- Conduct remote monitoring.
- Participate in study start-up processes.
- Specialize in a therapeutic area.
- Mentor less experienced team members.
- Provide subject matter expertise.
- Complete additional assigned tasks.
Work Experience
- 2 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Career Advancement
- Career growth resources
Flexible Working
- Flexible work schedules
- Home office
Mental Health Support
- Therapeutic knowledge programs
Startup Environment
- Dynamic work environments
Company Vehicle
- Company car
Other Benefits
- Accident insurance
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
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