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This range is provided by i-Pharm Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
A$80,000.00/yr - A$100,000.00/yr
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Principal Consultant at i-Pharm Consulting | Recruiting Clinical Operations, Clinical Project Management and Biometrics Professionals across Australia
Clinical Data Manager (Australia)
Join a dynamic, forward-thinking team and play a pivotal role in shaping the future of clinical research.
We are seeking an experienced Clinical Data Manager to oversee all aspects of the global clinical data management process—from study start-up to database lock and regulatory submission support. This opportunity is with a leading organisation in the life sciences sector, committed to innovation and excellence in healthcare. They are a growing business and so presents a lot of opportunities to grow and progress within the business.
They are seeking someone confident working independently and able to hit the ground running.
Why Choose Them?
* Cutting-edge technology: Work with Oracle, Veeva, and Medidata platforms in a cloud-enabled, secure environment.
* Hybrid/flexible working: Enjoy the autonomy to work remotely reflecting the latest trends in clinical research and data management.
* Professional growth: Access ongoing training, certifications, and a clear path for career advancement.
* Collaborative culture: Be part of a supportive, cross-functional team that values your expertise and encourages work-life balance.
* Meaningful impact: Your work ensures clean, reliable data that drives medical breakthroughs and improves patient outcomes.
Key Responsibilities
* Manage the clinical data lifecycle: Oversee data collection, cleaning, validation, and reporting for global clinical studies.
* Collaborate with CROs and vendors: Define and implement data management requirements, ensuring quality, compliance, and timely delivery.
* Drive data quality: Participate in eCRF design, database UAT, and ongoing data cleaning. Identify trends, suggest queries, and support continuous improvement.
* Support regulatory submissions: Prepare and validate data for clinical study reports and regulatory documentation.
* Project leadership: Track database lock timelines, manage project milestones, and report progress to management.
* Audit and inspection readiness: Contribute to audit preparation and inspection activities as required.
What We're Looking For
* Education: Bachelor's degree in a science/health-related field (or equivalent experience).
* Experience: Minimum 3 years in clinical data management, including vendor oversight.
* Technical skills: Working knowledge of CDISC/SDTM; Oracle experience required (Veeva and Medidata highly desirable).
* Soft skills: Outstanding communication, time management, and the ability to work both independently and as part of a small team.
* Adaptability: Willingness to learn new technologies and embrace evolving industry standards.
How to Apply
Please apply directly here or contact Keeley Munday at
Coversheets not required - CV is fine
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Research and Science
* Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
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