Senior Principal Research Coordinator

2 weeks ago

Sydney, New South Wales, Australia beBeeClinicalResearch Full time $90,000 - $120,000
Job Title: Senior Clinical Research Associate

As a Senior Clinical Research Associate, you will play a vital role in ensuring the success of clinical trials by delivering high-quality results and maintaining compliance with regulatory requirements.

Key Responsibilities:
  • Clinical Monitoring and Site Management: Perform and coordinate all aspects of the clinical monitoring and site management process to ensure trial integrity.
  • Protocol and Regulatory Compliance: Conduct remote or on-site visits to assess protocol and regulatory compliance, and manage required documentation.
  • Procedure Management: Manage procedures and guidelines from different sponsors and/or monitoring environments to guarantee subjects' rights, well-being, and data reliability.
Requirements:
  • Education and Experience: Bachelor's degree in a life sciences-related field or Registered Nursing certification, with a minimum of 4 years' experience in independent monitoring.
  • Therapeutic Experience: Essential therapeutic experience in Oncology, including Phase I experience.
What We Offer:
  • Competitive Remuneration Package: A comprehensive benefits package, including annual incentive plan bonus, comprehensive benefits, wellness programs, and an Employee Assistance Program.
  • Flexible Work Arrangements: Opportunities for flexible work arrangements, including paid birthday leave and company-paid parental leave.
  • Continuous Learning: Access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.

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