eSource Data Specialist (Clinical Trials)

University of the Sunshine Coast

Mons

On-site

AUD 50,000 - 71,000

Full time

4 days ago
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Benefits offered by this job

Casual opportunity
Athena SWAN Bronze Award
Modern teaching & research facilities

Job summary

UniSC Clinical Trials at UniSC Sunshine Coast invites applications for a Data Management Associate (eSource). This casual role focuses on developing and managing electronic source documentation across trial sites, translating CRFs and EDC outputs into source records, and providing system support.

You will engage with data management teams, trial sites, and software partners to deliver compliant, high-quality data management solutions and participate in audits and regulatory activities.

Qualifications

  • Relevant qualifications, training and/or experience.
  • Excellent organisational skills and attention to detail.
  • Strong written and verbal communication with stakeholders.
  • Ability to work independently and in a multidisciplinary team.

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

Attention to detail
Communication skills
Independent worker

Tools

EDC systems

Job description

UniSC Clinical Trials at UniSC Sunshine Coast invites applications for a Data Management Associate (eSource). This casual role focuses on developing and managing electronic source documentation across trial sites, translating CRFs and EDC outputs into source records, and providing system support.

You will engage with data management teams, trial sites, and software partners to deliver compliant, high-quality data management solutions and participate in audits and regulatory activities.

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