Clinical Research Associate

4 weeks ago

Sydney, New South Wales, Australia Pharmiweb Full time
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team in the Oncology Trials department. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.

Key Responsibilities
  • Monitor and manage clinical trials, including site initiation, interim monitoring, and close-out visits
  • Ensure compliance with GCP and regulatory requirements, including ICH guidelines and local regulations
  • Develop and maintain strong relationships with site staff, investigators, and other stakeholders
  • Provide training and support to site staff on study protocols and procedures
  • Conduct quality control checks on study data and documents
  • Collaborate with cross-functional teams to ensure timely and successful trial execution
Requirements
  • Bachelor's degree in a life science or related field
  • Minimum 2-3 years of experience in clinical research, preferably in Oncology trials
  • Strong knowledge of GCP, ICH guidelines, and local regulations
  • Excellent communication and interpersonal skills
  • Ability to work independently and as part of a team
  • Strong analytical and problem-solving skills
What We Offer
  • Competitive salary and benefits package
  • Opportunities for professional growth and development
  • Collaborative and dynamic work environment
  • Recognition and rewards for outstanding performance

We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.

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