Thermo Fisher Scientific·1 month ago
1 month ago
Clinical Research Associate II (FSP)
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What you'll do
- Support clinical monitoring and site management
- Ensure protocol and regulatory compliance
- Conduct site visits
- Review data
- Maintain documentation
What they're looking for
- Experience in clinical research monitoring
- Background in life sciences or nursing
- Bachelor's degree in life sciences
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
We are looking for a Clinical Research Associate II to support clinical monitoring and site management, ensuring protocol and regulatory compliance. You will conduct site visits, review data, and maintain documentation. Ideal candidates have experience in clinical research monitoring and a background in life sciences or nursing.
Skills
- clinical monitoring
- ich gcp
- bachelor's degree in life sciences
- risk based monitoring
- root cause analysis
- regulatory compliance
- clinical trial management system
- sdr
- sdv
- crf review
- investigator site management
- medical terminology
- clinical research
- project management
- business writing
- investigator identification
- trial close out
- file review
- process improvement
- regulatory audit response
- investigator payment process
- team collaboration
- oral communication
- written communication
Company
Thermo Fisher Scientific
Melbourne, Australia
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