clinical data manager

Clinical Data Management Specialist

Melbourne | Hybrid Working

We're partnering with a growing Australian CRO where Data Management is seen as a key contributor to study success, not just a support function. Here, you'll work closely with sponsors, project teams, and clinical operations colleagues from study start-up through to database lock, giving you the opportunity to see the real impact of your work on every project.

This is the kind of environment where people know your name, value your expertise, and trust you to make decisions.

Why this role is different

In larger organisations, it's easy to become highly specialised and disconnected from the wider study team.

In this role, you'll be part of a collaborative group where you'll have genuine involvement across the clinical trial lifecycle. You'll partner directly with stakeholders, contribute to study discussions, and play an important role in shaping how data is collected, managed, and delivered.

You'll have the autonomy to take ownership of your work while still having access to experienced colleagues who are happy to share knowledge and support your growth.

What you'll be doing

You'll be involved in a broad range of clinical data management activities, including:

• Supporting study start-up activities and database development

• Designing and maintaining electronic data capture systems

• Working closely with sponsors, vendors, and internal study teams

• Driving data quality through review processes and validation checks

• Managing ongoing database updates throughout study conduct

• Supporting database lock and close-out activities

• Providing guidance and expertise on data collection and management best practice

• Contributing ideas that improve processes, quality, and efficiency

What we're looking for

You'll likely bring:

• Experience within Clinical Data Management gained in a CRO, sponsor, or clinical research environment

• Hands-on experience with EDC platforms such as Medidata Rave, Viedoc, REDCap, or similar

• A strong understanding of clinical trial processes and data quality principles

• The confidence to engage with a variety of stakeholders

• A naturally curious and problem-solving mindset

• A desire to continue learning and expanding your responsibilities

What you'll get in return

This is an opportunity to join a company that's large enough to deliver global projects, but small enough that individual contributions are recognised and valued.

You'll enjoy:

• Meaningful involvement in end-to-end clinical studies

• Direct access to experienced leaders and decision-makers

• Broad exposure across therapeutic areas and project types

• A collaborative, down-to-earth culture where people genuinely support each other

• The opportunity to grow your career as the organisation continues to expand

• Flexibility and trust, with a focus on outcomes rather than micromanagement

Apply direct or contact Keeley Munday

••••@i-pharmconsulting.com

04•••••037