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Senior Clinical Research Associate

$110.52k - $138.15k

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This role involves overseeing clinical trial monitoring activities for Phase I oncology studies across New York and New Jersey sites. The Senior CRA will manage site compliance with protocols and regulatory standards, conduct site visits, mentor staff, and coordinate cross-functional teams to ensure data integrity and trial execution. Requires a bachelor's degree in a scientific field, extensive clinical research experience, and willingness to travel approximately 60% of the time.

Responsibilities

  • Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
  • Conduct site visits to assess performance, troubleshoot issues, and provide operational support
  • Collaborate with cross-functional teams on accurate data collection and reporting
  • Train site staff and other CRAs to maintain high standards of trial conduct
  • Build and maintain relationships with site personnel to support trial operations

Requirements

  • Bachelor's degree in scientific or healthcare-related discipline
  • Extensive clinical research associate experience with knowledge of trial processes
  • Ability to manage multiple sites and projects with strong organizational skills
  • Expertise in monitoring practices, data integrity, and site management
  • Proficiency in clinical trial software and relevant tools
  • Excellent communication and stakeholder management abilities
  • Willingness to travel approximately 60% of the time

Compensation: $110,520-$138,150 base

Vacancy posted a month ago
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