Senior Site Monitor

1 week ago

Sydney, New South Wales, Australia beBeeClinicalResearch Full time $120,000 - $150,000
Clinical Research Associate

Job Summary

We are seeking an experienced Clinical Research Associate to join our team. As a key member of our organization, you will be responsible for monitoring clinical trial sites and ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice standards.

Key Responsibilities:

  • Monitoring clinical trial sites to ensure compliance with regulations and company standards.
  • Conducting site visits to assess site performance and provide support as needed.
  • Collaborating with cross-functional teams to ensure timely data collection and reporting.
  • Providing training and guidance to site staff to maintain high standards of clinical trial conduct.
  • Fostering effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Requirements:

  • Bachelor's degree in life sciences or related field.
  • At least 2 years of experience as a Clinical Research Associate with a strong understanding of clinical trial processes and regulatory requirements.
  • Located in Central, West, or East regions.
  • Minimum of 12 months of independent monitoring experience.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

Therapeutic Areas:

  • Oncology-Solid Tumor
  • Gen Med-Complex Multiple Therapeutics: Vaccines, NASH/MASH, Cardio, Diabetes

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