Clinical Research Associate II/Senior CRA- Midlands
3 weeks ago
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits
- Ensure compliance with study protocols, GCP, and applicable regulatory guidelines
- Perform source data verification and review study documents
- Track and report patient enrollment and study progress
- Monitor study drug supply and accountability
Requirements:
- Bachelor's degree in a health-related field or equivalent
- 2+ years of Onsite monitoring
- Good understanding of clinical trial processes and regulatory requirements
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Competitive salary
- competitive benefits
- Car allowance
E:
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