Senior Clinical Research Associate
usd108.58k - usd135.72k per yearICON
ICON seeks a Clinical Research Associate to monitor clinical trials at investigative sites or remotely, ensuring studies are conducted and reported in accordance with protocols, SOPs, ICH-GCP guidelines, and applicable regulations.
Responsibilities
- Monitor progress of clinical studies at investigative sites or remotely
- Ensure clinical trials are conducted and documented per protocol and SOPs
- Verify compliance with ICH-GCP and applicable regulatory requirements
- Prepare and submit study reports according to established standards
Requirements
- Bachelor's degree in scientific or health-related field, or equivalent education and clinical research experience
- 1+ years clinical monitoring experience for level 2 role; 3+ years for level 3 role
- Knowledge of ICH and local regulatory authority regulations for drug trials
- Oncology monitoring experience preferred
- Ability to travel 70%
- Legal authorization to work in United States or Canada; no visa sponsorship required
Vacancy posted 1 day ago
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