Clinical Research Associate Specialist

1 day ago


Adelaide, South Australia Pharmiweb Full time
Job Description:

As a Clinical Research Associate II, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Key Responsibilities:

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborate with investigators and site staff to facilitate smooth study conduct.
  • Perform data review and resolution of queries to maintain high-quality clinical data.
  • Contribute to the preparation and review of study documentation, including protocols and clinical study reports.


Requirements:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Excellent communication skills in English.


What We Offer:

  • Competitive salary and annual leave entitlements.
  • Range of health insurance offerings and retirement planning.
  • Global Employee Assistance Programme and life assurance.
  • Flexible country-specific optional benefits.


About Us:

  • We foster an inclusive environment driving innovation and excellence.
  • Our rich diversity makes us more innovative, better serving our people, patients, customers, and communities.
  • We provide a workplace free of discrimination and harassment.


Equal Opportunities:
At ICON, we promote equal opportunities and strive to be an inclusive workplace. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, please let us know or submit a request.

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