Barmherzige Schwestern Krankenhaus Wien
Studienkoordinator:in / Study Nurse(m/w/x)
Full-time/Part-timeOn-siteExperienced
Wien
from 3,271 / month
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Liaising between Sponsor/CROs and clinical study sites for stronger study delivery, managing monitoring visits and patient enrollment at a Site Enabling Services organization. University degree in Life Science (pharmacy, nursing, lab analytics) preferred. Flexible working hours.
Requirements
- University degree in Life Science, preferably pharmacy, nursing or lab analytics
- Minimum 2 years on-the-job experience as site coordinator
- Ability to work in fast-paced environment with short timelines
- Effective communication in stressful situations and problem-solving ability
- Flexibility in working hours
- Fluent English and Local Language
Tasks
- Liaise between the Sponsor/CRO and the site.
- Ensure timely responses to feasibility questions.
- Assist with scheduling and preparing for monitoring visits.
- Respond to monitors during monitoring visits.
- Track patient enrollment.
- Support teams in meeting project timelines.
- Support teams in achieving enrollment goals.
- Maintain study-specific and general document tracking.
- Perform timely and accurate data entry into EDC systems.
- Resolve data clarification queries promptly.
- Report adverse events and protocol deviations promptly.
- Follow up on adverse events and protocol deviations promptly.
- Manage investigational products and clinical supplies properly.
- Collect, handle, and maintain site-specific regulatory documents.
- Facilitate and support site contract and budget negotiations.
- Support Investigator and site payment processes.
- Schedule and perform study procedures as required.
- Prepare for study audits and regulatory inspections.
- Participate in study audits and regulatory inspections.
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible working hours
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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Liaising between Sponsor/CROs and clinical study sites for stronger study delivery, managing monitoring visits and patient enrollment at a Site Enabling Services organization. University degree in Life Science (pharmacy, nursing, lab analytics) preferred. Flexible working hours.
Requirements
- University degree in Life Science, preferably pharmacy, nursing or lab analytics
- Minimum 2 years on-the-job experience as site coordinator
- Ability to work in fast-paced environment with short timelines
- Effective communication in stressful situations and problem-solving ability
- Flexibility in working hours
- Fluent English and Local Language
Tasks
- Liaise between the Sponsor/CRO and the site.
- Ensure timely responses to feasibility questions.
- Assist with scheduling and preparing for monitoring visits.
- Respond to monitors during monitoring visits.
- Track patient enrollment.
- Support teams in meeting project timelines.
- Support teams in achieving enrollment goals.
- Maintain study-specific and general document tracking.
- Perform timely and accurate data entry into EDC systems.
- Resolve data clarification queries promptly.
- Report adverse events and protocol deviations promptly.
- Follow up on adverse events and protocol deviations promptly.
- Manage investigational products and clinical supplies properly.
- Collect, handle, and maintain site-specific regulatory documents.
- Facilitate and support site contract and budget negotiations.
- Support Investigator and site payment processes.
- Schedule and perform study procedures as required.
- Prepare for study audits and regulatory inspections.
- Participate in study audits and regulatory inspections.
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible working hours
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
Healthcare
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?
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