Hybrid AU Clinical Data Associate: Data Quality & Trials

Novotech; Sydney; Hybrid; AUD 65,000 - 80,000; Full time

Job summary

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.

Qualifications

• Graduate in a clinical or life sciences field.
• Experience in allied professions may be considered.
• Preferably 6–12 months in research/pharma.

Responsibilities

• Data entry of clinical trial data using CDM software.
• Assist in review of data queries with sponsor staff.
• Track CRF pages and data queries.
• Support database testing and edit checks testing.
• Assist with data cleaning, validation and reconciliation.
• Maintain communications with lead CDMs.
• Create reports/listings as required.
• Coordinate coding and electronic data transfers as needed.
• Develop tracking systems for study progress (e.g., Novotrak).
• Participate in project meetings and assist with minutes.

Skills

Data entry

Clinical data management

GCDMP

Education

Graduate degree in life sciences

Tools

CDM software

Job description

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.