Study Coordination Specialist

1 week ago

Sydney, New South Wales, Australia beBeeClinical Full time $90,000 - $140,000

About Clinical Study Start Up

At our company, diverse teams enable us to become better partners to customers and advance patient lives.

We foster an "Own It" culture driven by accountability, collaboration, partnership, and integrity. We strive to deliver excellence in clinical research and be the partner of choice in drug development.

In this dynamic environment, you'll assist in developing country and site distribution plans and executing activities related to study start up. Our collaborative culture empowers us to achieve industry-leading results.

The Role

  • Perform feasibility assessments, identify sites, negotiate contracts, and execute other study start up activities.
  • Provide expertise on study start up to team leads and project teams.
  • Prepare and coordinate submissions to regulatory, ethics, and other bodies.
  • Develop, finalize, and review Master and Country Specific Subject Information Sheets/Informed Consent Forms.

Requirements

  • Bachelor's Degree or equivalent from a Medical/science background is required.
  • Minimum 1-2 years of experience in study start up requirements and activities are necessary.
  • Previous experience as a site coordinator working on clinical trials, including CRF entry at site, is preferred.
  • Fluency in English and local language is essential.

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