Site Management Professional

7 giorni fa


Milano, Lombardia, Italia Novasyte A tempo pieno

**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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