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12244en
- Contract
- English, German
- Associate
- Research & Development
- Zug
- Healthcare & Life Sciences
Skills
Clinical Research, Monitoring
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For our client, an International firm within the Healthcare & Life Sciences based in Rotkreuz, Swisslinx is seeking a highly motivated individual to take on a challenging role as a Clinical Research Associate. This is a great opportunity to bring your proven knowledge and expertise to an organization that offers a dynamic working environment.
Job Title: Clinical Research Associate
Duration: 12 months
Your mission:
- Participate in the design, planning, implementation and overall direction of clinical research projects
- Travel to field sites to monitor studies
- Work with Study Manager, Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
- Assume responsibility for training and coordinating certification of study site personnel
- Monitor the sites and provides technical assistance, as necessary
- Manage material logistics for the studies
- Ensure site compliance with regulations and study protocol
Your background:
- Bachelor in a technical or life science
- Minimum 1 year of experience as a Clinical Research Asociate
- Excellent skills in basic computer applications (Word, Excel, Access, PowerPoint)
- Excellent writing and verbal communication skills in German AND English
- Willing to work hands on in a laboratory with infectious material
- Experience in a hands-on work in laboratory, ideally with Polymerase Chain Reaction (PCR) methods
Job Title: Clinical Research Associate
Duration: 12 months
Your mission:
- Participate in the design, planning, implementation and overall direction of clinical research projects
- Travel to field sites to monitor studies
- Work with Study Manager, Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
- Assume responsibility for training and coordinating certification of study site personnel
- Monitor the sites and provides technical assistance, as necessary
- Manage material logistics for the studies
- Ensure site compliance with regulations and study protocol
Your background:
- Bachelor in a technical or life science
- Minimum 1 year of experience as a Clinical Research Asociate
- Excellent skills in basic computer applications (Word, Excel, Access, PowerPoint)
- Excellent writing and verbal communication skills in German AND English
- Willing to work hands on in a laboratory with infectious material
- Experience in a hands-on work in laboratory, ideally with Polymerase Chain Reaction (PCR) methods
