Clinical Data Manager

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 kmunday@i-pharmconsulting.com

Coversheets not required - CV is fine!