IQVIA
Clinical Research Associate I or II(m/w/x)
Full-timeWith HomeofficeJunior
Wien
from 3,600 / month
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PSPSI CRO
Site Identification Specialist(m/w/x)
Wien
from 70,000 / year
Full-timeWith Home OfficeJunior
Nejo AI Summary
Strategic relationship building and database refinement for clinical trial center selection at global CRO. University degree in MD or PharmD and advanced English skills required. On-site monitoring experience preferred.
Requirements
- University/college degree (MD/PharmD) or equivalent education, training, and experience
- On-site monitoring experience (plus)
- Understanding of Good Clinical Practice, local laws, and regulations
- Ability to work in dynamic environment, under compressed deadlines
- Advanced English skills
Tasks
- Communicate with clinical sites
- Build relationships with clinical sites
- Identify potential centers for clinical trials
- Maintain and refine internal site databases with cross-functional teams
- Conduct site identification activities during startup
- Discuss clinical trial protocols
- Collect site identification questionnaires
- Define study objectives and optimal site profiles
- Create initial lists of potential sites
- Refine site contact strategy with project teams
- Refine site contact methodology with project teams
- Maintain study site identification tracker with the project team
- Evaluate site identification progress with project teams
- Identify and highlight risks to timelines or objectives
- Conduct due diligence checks with Legal
- Evaluate regulatory and legal limitations for sites
- Evaluate regulatory and legal limitations for investigators
- Support project teams during study startup
- Provide support for additional site identification rounds
- Gather additional site or investigator information
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Competitive Pay
- Fair and attractive salary
Other Benefits
- Excellent working conditions
Informal Culture
- Supportive and collaborative environment
- Friendly, professional team
Learning & Development
- Extensive training
Career Advancement
- Personal and professional growth opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of PSI CRO and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Clinical Site Management Lead(m/w/x)
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Clinical Research Associate 2(m/w/x)
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PSPSI CRO
Site Identification Specialist(m/w/x)
Wien
from 70,000 / year
Full-timeWith Home OfficeJunior
Nejo AI Summary
Strategic relationship building and database refinement for clinical trial center selection at global CRO. University degree in MD or PharmD and advanced English skills required. On-site monitoring experience preferred.
Requirements
- University/college degree (MD/PharmD) or equivalent education, training, and experience
- On-site monitoring experience (plus)
- Understanding of Good Clinical Practice, local laws, and regulations
- Ability to work in dynamic environment, under compressed deadlines
- Advanced English skills
Tasks
- Communicate with clinical sites
- Build relationships with clinical sites
- Identify potential centers for clinical trials
- Maintain and refine internal site databases with cross-functional teams
- Conduct site identification activities during startup
- Discuss clinical trial protocols
- Collect site identification questionnaires
- Define study objectives and optimal site profiles
- Create initial lists of potential sites
- Refine site contact strategy with project teams
- Refine site contact methodology with project teams
- Maintain study site identification tracker with the project team
- Evaluate site identification progress with project teams
- Identify and highlight risks to timelines or objectives
- Conduct due diligence checks with Legal
- Evaluate regulatory and legal limitations for sites
- Evaluate regulatory and legal limitations for investigators
- Support project teams during study startup
- Provide support for additional site identification rounds
- Gather additional site or investigator information
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Competitive Pay
- Fair and attractive salary
Other Benefits
- Excellent working conditions
Informal Culture
- Supportive and collaborative environment
- Friendly, professional team
Learning & Development
- Extensive training
Career Advancement
- Personal and professional growth opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of PSI CRO and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
PSI CRO
Industry
Research
Description
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Not a perfect match?
- IQVIA
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