Clinical Research Associate

3 weeks ago

Canberra, ACT, Australia Pharmiweb Full time
Job Summary

As a Clinical Research Associate at Pharmiweb, you will be responsible for monitoring pharmaceutical industry clinical trials, with a focus on Oncology trials. This role requires a strong understanding of Good Clinical Practice, ICH guidelines, and local regulatory requirements.

Key Responsibilities
  • Monitor multiple trials within Oncology, ensuring compliance with regulatory requirements and Good Clinical Practice guidelines.
  • Develop site start-up documents, including SIV agendas, and provide training to site staff.
  • Act as a Lead SM, training other SMs on study protocols and procedures.
  • Represent the company on Site Management Teams (SMTs) and meetings, ensuring effective communication and collaboration with site staff.
  • Travel up to 50% to conduct site visits and monitor trial progress.


Requirements
  • Bachelor's degree in Biological Sciences or equivalent.
  • Minimum 2-3 years' experience in monitoring pharmaceutical industry clinical trials.
  • Experience in Oncology trials is highly desirable.
  • Strong analytical and risk-based monitoring skills.
  • Ability to operate and use various systems and databases, including CTMS, EDC, eTMF, and IWRS.
  • Excellent communication and influencing skills, with the ability to work independently and as part of a team.


What We Offer
  • Competitive salary range: $89,376.00 - $111,720.00 USD.
  • Annual leave entitlements, health insurance, retirement planning, and other benefits.
  • Opportunities for professional growth and development.


At Pharmiweb, we value diversity, inclusion, and belonging. We are committed to providing an inclusive and accessible environment for all candidates and employees. If you require reasonable accommodations during the application process, please let us know.

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