Site Management Professional
7 giorni fa
**Job Overview:**
Novasyte is a leading provider of clinical research services to the life sciences industry. We're seeking an experienced Site Management Professional to join our team in executing clinical studies.
**Key Responsibilities:**
- Perform site initiation, monitoring and close-out visits to ensure compliance with study protocols, regulations and sponsor requirements.
- Provide protocol training to assigned sites and establish regular communication lines to manage project expectations and issues.
- Evaluate the quality and integrity of study site practices related to protocol adherence and regulatory compliance, escalating quality issues as necessary.
- Manage study progress by tracking regulatory submissions, recruitment and enrollment, CRF completion and submission, and data query generation and resolution.
**Required Qualifications:**
- High School Diploma or equivalent degree in a scientific discipline or healthcare preferred.
- At least 2 years of on-site monitoring experience.
- Good knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
- Excellent therapeutic and protocol knowledge, proficiency in Microsoft Office and ability to communicate effectively in English.
- Organizational and problem-solving skills, effective time management and financial acumen.
**Salary Range:** $65,000 - $80,000 per annum, depending on experience.
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