Data Management Associate (eSource) - Casual

• UniSC Clinical Trials | UniSC Sunshine Coast, Sippy Downs
• Level 3, $43.98 per hour plus 12% superannuation
• Casual opportunity

Join UniSC Clinical Trials as a Data Management Associate (eSource) and play a key role in advancing clinical research through innovative digital data collection practices. You’ll support the development, implementation and ongoing management of electronic source documentation across our clinical trial sites, working collaboratively with clinical trial teams, data management specialists and software partners to deliver efficient, accurate and compliant data management solutions that support high-quality clinical research.

For more information, please visit us online: UniSC Clinical Trials

• 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.

You are a proactive and well-organised professional with strong attention to detail and excellent communication skills. You enjoy building positive working relationships, engaging with a range of stakeholders and contributing to a collaborative team environment. You are adaptable, solutions-focused and confident working independently, managing competing priorities and delivering accurate, high-quality outcomes. You bring a commitment to continuous improvement and the ability to approach challenges with initiative, professionalism and a strong focus on achieving results.

• 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; and
• The ability to work independently and collaboratively within a multidisciplinary team environment.

• Experience producing and managing source documentation within clinical research sites.
• Ability to interpret annotated CRFs and EDC outputs and translate these into source documentation.
• Understanding of clinical trial data management processes.

Don't meet every requirement? At UniSC, we understand that your work and life experiences can be just as valuable. If you're excited about this role but your CV doesn't align perfectly with our position description, we encourage you to apply anyway. You may be just the right candidate for this or one of our many other opportunities.

UniSC is an equal opportunity employer, committed to diversity and inclusion. We encourage applications from all backgrounds, including those with disabilities, women in STEM, First Nations Peoples, and individuals of diverse cultures, genders, abilities, and experiences. We value achievement relative to opportunity and encourage your commentary on your achievements in this context. For additional support during the application process, please contact us at unisc-careers@usc.edu.au or call +61 7 5430 2830.