Clinical Research Coordinator

2 weeks ago

Melbourne, Victoria, Australia beBeeClinicalResearch Full time $100,000 - $140,000
Job Overview

Clinical research professionals are responsible for overseeing the management and administration of clinical trials. Their key duties include preparing protocols and documents for trial approval, ensuring compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOP). They also monitor and coordinate clinical trial activities to ensure timely updates to electronic data capture (EDC)/clinical trial management system (CTMS) systems.

  • Prepare and submit trial-related documents to regulatory authorities.
  • Monitor and coordinate clinical trial activities.
  • Ensure timely updates to EDC/CTMS systems.
  • Report serious adverse events/adverse drug reactions.
Key Qualifications
  • Bachelor's degree in a biomedical or life sciences discipline.
  • A minimum of 3-10 years of experience in clinical operations monitoring.
  • Excellent communication and organizational skills.

Panacro Pharmaceutical Technology Co., Ltd. specializes in pharmaceutical R&D and clinical studies as a contract research organization.

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