Clinical Trial Research Support

University of Sydney; Sydney; Presencial; AUD 73.000 - 103.000; A tiempo parcial

Descripción de la vacante

The University of Sydney is offering a casual opportunity in the School of Health Sciences Administration to support clinical trials. The role focuses on data capture, data entry, and adherence to GCP and SOPs, with an emphasis on quality outcomes.

You will work under supervision, coordinating trial activities, engaging with stakeholders, and ensuring safety and regulatory compliance while developing professional skills in a supportive academic environment.

Formación

• Currently studying or completed a qualification in Health Sciences or related discipline.
• Knowledge of COPD or related conditions is preferred.
• Ability to work with others and manage competing priorities to meet deadlines.
• Excellent verbal and written communication, with quality customer service.
• High computer literacy and experience with data entry and record management.
• Strong organisational and time management skills.

Responsabilidades

• Coordinate and assist in various clinical trial activities under supervision.
• Lead data capture and entry to ensure accuracy and compliance with GCP/SOPs.
• Review ethics guidelines, WHS requirements and trial standards.
• Develop relationships with clinical trial stakeholders and facilitate communication.
• Prioritise health and safety and participate in safety drills and training.

Conocimientos

Health sciences

COPD knowledge

Communication skills

Data entry

Time management

Team collaboration

Computer literacy

Educación

Health Sciences / related discipline

Descripción del empleo

Casual Opportunity providing clinical trial support within the School of Health Sciences Administration

HEO 5 Step 1 $63.90 per hour plus Super

PHD and Masters Students highly encouraged to apply

About the opportunity

The Clinical Trial Support Data Collection Officer plays an important role in supporting clinical trial activities, leading data capture and entry operations to ensure accuracy, integrity and compliance with regulatory requirements. The role also focuses on building strong relationships with key clinical trial stakeholders and contributing to quality outcomes by ensuring clinical trial procedures align with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs).

Your key responsibilities will be to:

• working under the supervision of the study coordinator and trial lead, you will actively contribute to various clinical trial activities, assisting in the coordination and operation of trial
• lead data capture and entry for a clinical trial, ensuring accuracy and compliance with Good Clinical Practice (GCP) and other relevant regulations
• review and enforce adherence to ethics guidelines, WHS requirements, and other relevant standards in the conduct of clinical trials
• develop and maintain strong relationships with clinical trial stakeholders, participating in research meetings and facilitating communication among various entities.
• lead by example in prioritising health and safety within daily operations, coordinate with peers for safety drills and training, and proactively identify areas for safety improvement within the work scope

About You

• Currently studying or completed a qualification in Health Sciences, Exercise Science, Exercise Physiology, Physiotherapy, or a related discipline.
• Knowledge of, or experience with the management of Chronic Obstructive Pulmonary Disease (COPD) or other similar conditions
• Demonstrated ability to work collaboratively and manage competing priorities to meet deadlines
• Effective verbal and written communication skills, with experience providing high-quality customer service and responding to a range of enquiries.
• High level of computer literacy and proficiency in common software applications
• Experience in accurate data entry and record management
• Strong organisational and time management skills
• A collaborative approach and commitment to working effectively within a team

Sponsorship / work rights for Australia

You must have unrestricted work rights in Australia for the duration of this employment to be eligible to apply. Visa sponsorship is not available for this appointment.

Pre-employment checks and declarations

Your employment is conditional upon the successful completion of all pre-employment or background checks required for the role in terms satisfactory to the University. Also, to meet the University's obligations under the National Higher Education Code to Prevent and Eliminate Gender-Based Violence you will be asked to declare if you have been investigated for, or found to engaged in, sexual harm or gender-based violence in the course of previous employment or in a legal process. Similarly, your ongoing employment is conditional upon the satisfactory maintenance of all relevant clearances and background check requirements. If you do not meet these conditions, the University may take any necessary step, including the termination of your employment.

EEO statement

At the University of Sydney, our shared values are trust, accountability and excellence and we strive to be a place where everyone can thrive. We are committed to creating a University community that thrives through diversity and reflects the wider community that we serve. We deliver on this through our commitment to diversity and inclusion , evidenced by our people and culture programs, as well as key strategies to increase participation and support the careers of Aboriginal and Torres Strait Islander People , women , people living with a disability , people from culturally and linguistically diverse backgrounds , and those who identify as LGBTQIA+ . We welcome applications from candidates from all backgrounds. We are proud to be recognised as an Australian Workplace Equality Index (AWEI) Platinum Employer. Find out more about our work on diversity and inclusion .