Thermo Fisher Scientific·14 days ago
14 days ago
CRA - FSP - Denmark
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What you'll do
- Support clinical trial monitoring and site management in Denmark
- Ensure protocol and regulatory compliance
- Manage documentation
- Collaborate with investigational sites
What they're looking for
- clinical monitoring
- ich-gcp compliance
- bachelor's degree in life sciences
- experience in clinical research monitoring
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
We are seeking a Clinical Research Associate (Level II) to support clinical trial monitoring and site management in Denmark. You will ensure protocol and regulatory compliance, manage documentation, and collaborate with investigational sites. Ideal candidates have experience in clinical research monitoring and strong organizational and communication skills.
Skills
- clinical monitoring
- ich-gcp compliance
- bachelor's degree in life sciences
- risk based monitoring
- root cause analysis
- sdr
- sdv
- crf review
- clinical trial management system
- regulatory compliance
- investigator site initiation
- trial close out
- medical terminology
- clinical research monitoring
- investigator site management
- business writing
- problem solving
- critical thinking
- investigator identification
- audit readiness
- investigator payment process
- project status reporting
- process improvement
- team collaboration
- presentation skills
Company
Thermo Fisher Scientific
Remote, Denmark
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