About us

Accelagen is a locally positioned and globally adept full-service Contract Research Organisation (CRO) headquartered in Melbourne. We partner with innovative clients across the globe to drive meaningful advancements in human health and wellness. With over 15 years of delivered success, our expertise spans across the health, wellness and disease spectrum.

We offer end-to-end services across Strategic Consultancy, Clinical Trials, Regulatory Affairs, Biometrics, Safety and Medical monitoring and Quality assurance, helping our clients deliver smarter, faster, and more impactful outcomes. About the Role

Accelagen is seeking a highly motivated Clinical Database Developer to join our growing Data Management team. In this role, you will be responsible for the planning, design, development, and maintenance of clinical study databases, ensuring the integrity, quality, and reliability of clinical trial data throughout the study lifecycle.

Working closely with sponsors, vendors, study teams, and internal stakeholders, you will play a key role in study start-up activities, CRF design, database development, validation programming, and ongoing database maintenance. Key Responsibilities

Clinical Database Development

Lead study start-up activities related to CRF design and database development.

Design and build electronic Case Report Forms (eCRFs) and study databases.

Configure user roles, permissions, and study workflows.

Define and program edit checks and validation rules.

Develop custom reports and system outputs as required.

Perform database testing, Go Live activities, mid-study updates, maintenance, and database closure.

Ensure structural consistency, integrity,



and quality of study data throughout the clinical trial lifecycle.

Data Management Operations

Act as subject matter experts on data capture and collection methods

Provide expertise in external data transfer methods

Train sponsors/site staff/vendors/internal staff on EDC systems and CRF completion

Deliver high-quality service to stakeholders.

About

You

You are an organised and detail-oriented professional who enjoys working in a collaborative environment and takes ownership of delivering high-quality outcomes.

You will bring

Strong verbal and written communication skills.

Excellent attention to detail and problem-solving abilities.

A proactive, solutions-focused approach The ability to manage competing priorities and work independently.

The ability to interpret and apply regulatory guidelines effectively.

Current knowledge of ICH-GCP and clinical research requirements.

Qualifications & Experience

Tertiary qualification in Science, Pharmacy, Life Sciences, or a related discipline.

Minimum 2 years' experience in clinical data management.

Certification in a relevant Electronic Data Capture (EDC) system (Viedoc and/or RAVE preferred)

Experience designing and maintaining clinical research databases.

Knowledge of clinical trial processes and data management principles.

Why Join

Accelagen?

At Accelagen, you'll be part of a collaborative and high-performing team supporting creative clinical research across a diverse range of therapeutic areas.

We offer opportunities for professional growth, flexible working arrangements, and the chance to make a meaningful impact on clinical trials that improve patient outcomes.

Ready to join us? Apply now and help shape the future of clinical research.

📌 Clinical Database Developer (Melbourne)
🏢 Accelagen
📍 Melbourne