eSource Data Steward, Clinical Trials (Casual)

UniSC Careers

Sunshine Coast Regional

On-site

AUD 50,000 - 71,000

Full time

5 days ago
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Benefits offered by this job

Collaborative culture
Modern facilities
Career development
Athena SWAN Bronze Award

Job summary

UniSC Clinical Trials on the Sunshine Coast is seeking a Data Management Associate (eSource) to develop and manage electronic source documentation across our clinical trial sites. You will work with trial teams, data management specialists and software partners to deliver compliant data management solutions.

The role involves translating CRFs, supporting EDC outputs, and contributing to audits and validation. This is a casual opportunity with a level 3 pay of $43.98 per hour plus 12% super.

Qualifications

  • Relevant qualifications, training and/or experience.
  • Excellent organisational skills and attention to detail.
  • Strong written and verbal communication skills and the ability to work effectively with a range of stakeholders.
  • The ability to work independently and collaboratively within a multidisciplinary team environment.

Responsibilities

  • Build, maintain and manage electronic source documents and eSource systems across the clinical trials network.
  • Translate annotated CRFs and EDC outputs into appropriate source documentation.
  • Provide technical support for the electronic source documentation system.
  • Support computer system validation, quality assurance and compliance activities.
  • Assist with audits and regulatory inspections relating to clinical trial systems and source documentation.
  • Collaborate with clinical trial sites, data management teams, clients, and software partners to deliver effective and innovative solutions.

Skills

Organisational skills
Attention to detail
Communication skills
Stakeholder collaboration

Education

Relevant qualifications

Job description

UniSC Clinical Trials on the Sunshine Coast is seeking a Data Management Associate (eSource) to develop and manage electronic source documentation across our clinical trial sites. You will work with trial teams, data management specialists and software partners to deliver compliant data management solutions.

The role involves translating CRFs, supporting EDC outputs, and contributing to audits and validation. This is a casual opportunity with a level 3 pay of $43.98 per hour plus 12% super.

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