Clinical Research Associate

2 weeks ago


Hobart, Tasmania, Australia Pharmiweb Full time
Clinical Research Associate Role

We are seeking a highly skilled Clinical Research Associate to join our team at Pharmiweb. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.

Key Responsibilities:
  • Site Qualification and Monitoring: Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Protocol Compliance and Data Integrity: Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Study Conduct: Collaborate with investigators and site staff to facilitate smooth study conduct.
  • Data Review and Resolution: Perform data review and resolution of queries to maintain high-quality clinical data.
  • Study Documentation and Reporting: Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
Requirements:
  • Education: Bachelor's degree in a scientific or healthcare-related field highly preferred.
  • Experience: Minimum of 2 years of experience as a Clinical Research Associate (on-site monitoring experience required).
  • Skills: In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail.
What We Offer:

At Pharmiweb, we offer a competitive salary and a range of benefits to support your well-being and work-life balance. Our benefits include various annual leave entitlements, health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme.

We are committed to providing an inclusive and accessible environment for all candidates. If you need a reasonable accommodation for any part of the application process, please let us know.



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