At a Glance
- Tasks: Support data management activities and ensure quality standards in clinical trials.
- Company: Join Novotech, a leading clinical research organisation with a collaborative spirit.
- Benefits: Flexible hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Dynamic team environment with potential for career advancement.
- Why this job: Make a difference in healthcare by ensuring data integrity in clinical trials.
- Qualifications: Life sciences background with some experience in pharma preferred.
The predicted salary is between 62100 - 75900 $ per year.
Novotech is seeking a Clinical Data Associate I to support day-to-day data management activities in a hybrid Sydney/Melbourne/Brisbane office setup.
The role involves data entry, data validation, and reconciliation to ensure SOP and ICH-GCP standards are met.
You will work with the Biometrics Project Manager, review data queries, track CRF pages, and help with database testing, coding coordination, and progress reporting.
A life sciences background with 6–12 months in pharma is preferred.
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Hybrid AU Clinical Data Associate: Data Quality & Trials in Sydney employer: Novotech
Novotech is an exceptional employer that fosters a dynamic and collaborative work culture, perfect for those passionate about advancing their careers in toxicology and regulatory affairs. Located in Australia, we offer our employees comprehensive growth opportunities, competitive benefits, and the chance to work alongside industry experts on cutting-edge projects in clinical trials. Join us to make a meaningful impact in the field while enjoying a supportive environment that values innovation and professional development.
