Clinical Trials Associate - Internal Only

UniSC Careers; Sunshine Coast Regional; On-site; AUD 83,000 - 93,000; Full time

Benefits offered by this job

17% Super

Flexible work arrangements

Athena SWAN Bronze Award

Discounted private health

Job summary

UniSC Careers is seeking a dedicated professional to join UniSC Clinical Trials on a full-time basis at UniSC South Bank, Brisbane. The role supports trial activities, ensures regulatory compliance, and coordinates with sponsors and monitors to uphold high-quality conduct of clinical trials.

Travel to sites and participation in on-call activities may be required. You will work within a dynamic team, possess strong computer literacy, and have a health science background.

Qualifications

• Degree qualification in Health Science/Bio-Medical Science or similar; or a certificate level qualification; or an equivalent combination of relevant experience, education, and training.
• Knowledge of ICH Good Clinical Practice highly regarded.
• Exercise sound judgement, take initiative and solve problems, as required.
• Strong computer literacy including proficiency with the Microsoft suite and experience with databases.
• Prior experience within a clinical research environment is preferred.

Responsibilities

• Support the Clinical Trials Coordinator (CTC) and other clinical trials staff with all HREC-approved protocol requirements across the clinical trial life cycle in accordance with appropriate training and experience.
• Work collaboratively with the UniSC Clinical Trials team, sponsors and monitors to ensure high quality and safe conduct of clinical trials conducted by UniSC CT.

Education

Health Science or related field

Tools

Microsoft Suite

Job description

• UniSC Clinical Trials | UniSC South Bank, South Brisbane
• Level 5, $82,843 - $93,358 p.a., plus up to 17% employer superannuation
• Full-time (36.25 hours per week), 2 year fixed-term appointment

The Opportunity

Join our team and play a vital role in advancing clinical research! As a key member of UniSC Clinical Trials, you’ll ensure all trial activities comply with ICH Good Clinical Practice, ethical protocols, UniSC Clinical Trials Standard Operating Procedures, and regulatory requirements. Your expertise will help drive high-quality, compliant research that makes a real impact. If you're passionate about clinical research excellence, we’d love to hear from you!

Please note, this role requires flexibility to travel to different clinical trial sites as needed, and to work outside standard business hours to support confinement studies and other time-sensitive trial activities. You may also be required to participate in a 24/7 on-call or confinement roster.

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

You will

• Support the Clinical Trials Co-ordinator (CTC)and other clinical trials staffwith all HumanResearch Ethics Committee (HREC)approved protocolrequirements across the clinical trial life cyclein accordance withappropriate trainingand experience; and
• Work collaboratively with the UniSC Clinical Trials (UniSC CT) team,sponsorsand monitors to ensure high quality and safe conduct of clinical trials conducted by UniSC CT.

About you

You’re a proactive problem-solver who exercises sound judgment and takes initiative when needed. With strong computer literacy, including advanced skills in the Microsoft Suite and experience with databases, you work efficiently and effectively. You thrive in dynamic environments, adapting quickly to new challenges while maintaining accuracy, attention to detail, and high-quality outcomes.

You will possess:

• Degree qualification in Health Science/Bio-Medical Science orsimilar; ora certificate level qualification; or an equivalent combination of relevant experience, education, and training;
• Knowledge of ICH Good Clinical Practicehighly regarded;
• Exercise sound judgement, take initiative and solve problems, asrequired;
• Strong computer literacy includingproficiencywith the Microsoft suite of tools and experience with software programsincluding databases; and
• Prior experience within a clinical research environment is preferred.

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 [e-mail] or call [phone].

UniSC values a diverse and talented workforce and invites applications from candidates who already have legal work rights in Australia.

Our Culture & Benefits:

• Our collaborative, passionate and welcoming culture is what really sets us apart.
• Modern teaching & research facilities.
• Professional development and career pathway opportunities.
• We are a proud recipient of the prestigious Athena SWAN Bronze Award, granted as part of theScience in Australia Gender Equity (SAGE)initiative.
• Flexible work arrangements & generous leave options.
• Salary packing options + 17% Super.
• EAP, fitness passport & discounted private health.