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About the Role
Supports the day-to-day operations of data management projects, providing in-house data entry and administrative support to Clinical Data Managers (CDMs) according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs.
Responsibilities
- Performs data entry of clinical trial data using Clinical Data Management software.
- Assists in reviewing data queries for potential submission to sponsors or monitoring staff.
- Tracks CRF pages received and entered, as well as data queries sent, received, and entered.
- Supports CDMs with database testing and edit checks testing.
- Assists CDMs with data cleaning, validation, and reconciliation of external data.
- Develops and maintains effective communication and working relationships with lead CDMs.
- Helps CDMs create reports, listings, and other outputs as needed during projects.
- May coordinate activities related to coding and electronic data transfers, addressing discrepancies.
- Assists with the development and updating of systems to track study progress (e.g., Novotrak, CRF & query flow, safety reports).
- Provides study progress updates to CDMs.
- Participates in project meetings as requested by CDMs.
- Assists with agenda and minute writing for data management teams.
Requirements
- Graduate in a clinical or life sciences related field.
- Relevant experience/qualifications in allied professions may be considered.
- Preferably at least six months to one year of experience in research, the pharmaceutical industry, or a related field.
Experience Level
- Six months to one year experience
Education Level
- Graduate in a clinical or life sciences related field
Benefits
- Flexible benefits framework (NovoLife)
About the Company
- Novotech is a global full-service clinical Contract Research Organization (CRO).
- Novotech is a globally recognized leader in clinical research and scientific advisory services.
- Award-winning workplace culture that values ambition, innovation, and growth.
- Named Employer of Choice, Great Place to Work, and Employer of Choice for Gender Equality (EOCGE).
- Committed to fostering an environment that reflects life-changing work.
- Expanded global footprint with 30+ offices across Asia-Pacific, the United States, and Europe.
- Unites professionals from diverse backgrounds to advance therapies.
- Offers trust, flexibility, and autonomy.
- Provides access to mentorship opportunities and professional development programs.
- Offers a platform for personal growth and shaping the future of healthcare.
- Possesses advanced therapeutic and regulatory expertise.
- Demonstrates ability to execute across markets.
- Employs a client-centric service model.
- Provides a trusted, long-term partner and an accelerated path to market for clients.
- Offers opportunities to develop careers in a diverse and supportive global organization with a collaborative culture.
- Works with clients on the cutting-edge of life sciences.
- Features empowered teams with a shared commitment to success.
- Values a strategic vs. transactional mindset.
- Encourages the ability to gain insights and make proactive decisions quickly.
- Fosters a culture of partnership and collaboration where every voice is heard and valued.
- Provides ongoing support from senior stakeholders and the leadership team.