At a Glance
- Tasks: Support data management projects and ensure quality standards in clinical studies.
- Company: Join a leading clinical research organisation with a focus on innovation.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative team environment with potential for career advancement.
- Why this job: Make a difference in healthcare by managing critical clinical trial data.
- Qualifications: Graduate in clinical or life sciences; experience in research is a plus.
The predicted salary is between 81000 - 99000 $ per year.
Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech/Client SOPs.
This Hybrid role will be based 2 days in the Sydney, Melbourne or Brisbane office.
Responsibilities
- Member of the project team reporting to the Biometrics Project Manager on projects, the Clinical Data Associate I is responsible for providing accurate data acquisition, data validation and reconciliation to the clinical studies and shall ensure quality standards per SOPs and ICH-GCP.
- Data entry of clinical trial data using Clinical Data Management software.
- Assistance in review of data queries to be raised with sponsor companies/monitoring staff.
- Tracking of CRF pages received and entered, tracking of data queries sent received and entered.
- Assist CDM with database testing and edit checks testing as appropriate.
- Assist CDM with data cleaning/validation and reconciliation of external data
- Develop and maintain good communications and working relationships with lead CDMs.
- Assist CDM to create reports, listings, and other output as required during the course of the project.
- May coordinate activities related to coding and electronic data transfers, and address resulting discrepancies.
- Assist with the development and update of systems to track study progress as per the CDM requirements (i. e.
Novotrak, CRF & query flow, safety reports, etc.).
Provide updates on study progress to CDM as required.
- Participation in project meetings as requested by CDM.
- Assist with agenda/minute writing for data management teams.
Minimum Qualifications & Experience
- Graduate in a clinical or life sciences related field.
- Relevant experience/qualifications in allied professions may also be considered.
- Preferably at least six months to one year experience working in the research, pharmaceutical industry or a related field.
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Clinical Data Associate – Australia 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.
