Job Description
The Opportunity
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We are partnering with an established clinical research organisation seeking an experienced Clinical Database Developer or Senior Clinical Database Developer to join its Data Management team. This is a hands-on role for someone with strong experience in clinical database development, eCRF design and EDC systems, who enjoys working across the full study lifecycle from study start-up and database build through to go-live, maintenance and database close. For candidates operating at Senior level, the role will also provide the opportunity to act as a technical expert, support the development of database standards and mentor other team members.
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You will be responsible for:
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Leading clinical database activities during study start-up
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Designing and developing eCRFs and clinical study databases
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Translating study protocols into effective data capture solutions
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Developing and programming validation/edit checks
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Configuring user roles and system access
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Creating study-specific reports
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Managing database go-live activities
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Performing mid-study database changes and maintenance
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Supporting database close and study completion activities
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Ensuring data structures are consistent, accurate and fit for purpose
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Providing expertise in clinical data capture and external data transfers
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Training sponsors, sites,



vendors and internal teams in EDC systems and CRF completion
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Working closely with Clinical Operations, Biometrics, Data Management teams, clients and external vendors
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About you:
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A tertiary qualification in Science, Pharmacy or a related technical discipline
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At least 2 years' experience in clinical data management for the Clinical Database Developer level
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For Senior level, at least 4 years' clinical data management experience, including a minimum of 2 years developing clinical databases
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Certification in a relevant EDC platform
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Demonstrated hands-on experience building clinical study databases
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Experience designing eCRFs and developing validation/edit checks
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Strong knowledge of clinical research processes and ICH-GCP
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An understanding of regulatory requirements relating to clinical trials
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Robust attention to detail and quality
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Excellent written and verbal communication skills
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The ability to work independently, prioritise effectively and proactively resolve issues.
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Why consider this opportunity?
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This is a great opportunity for an experienced clinical data professional who enjoys the technical/database development side of clinical research and wants to work across a varied portfolio of clinical studies.

📌 Clinical Database Developer (Victoria)
🏢 Healthcare Professionals Group
📍 Victoria