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Clinical Research Associate II
2 months ago
Key Responsibilities
Conducts remote and on-site monitoring visits and documents findings
Ensures compliance with protocols, SOPs, ICH GCP, and regulatory requirements
Provides training to site staff and facilitates resolution of action items post-visit
Required Qualifications
Bachelor's degree in a scientific discipline or equivalent work experience
1-2 years of relevant monitoring experience (on-site and remote)
Proficient with MS Office Suite
Knowledgeable in clinical research operations and ICH guidelines
Ability to work independently and collaboratively in a team-oriented environment