Clinical Trial Coordinator – Adolescent Knee Pain

Vor 2 Tagen

Brisbane, Österreich Researchmanagement Vollzeit

Clinical Trial Coordinator – Adolescent knee pain
Apply locations St Lucia Campus time type Part time posted on Posted 17 Days Ago job requisition id R-46605
School of Health and Rehabilitation Sciences
Part-time (40% FTE), fixed-term position for 2 years (through to 31 March 2027)
The full-time base salary will range from $89,861 - $96,402 + 17% Superannuation (HEW Level 6)
Primarily based at our St Lucia campus
About This Opportunity We are seeking a highly motivated and organised Clinical Trial Coordinator to provide clinical trial coordination and implementation of a multi-centre clinical trial entitled ACTIVE KNEECAPs
Led by Associate Professor Natalie Collins, this project is funded by the Medical Research Future Fund (MRFF) and aims to provide healthcare practitioners with the evidence and resources to make informed treatment decisions for adolescents with kneecap pain.
Reporting to the Clinical Trial Manager, this position encompasses a broad range of research-related activities, including project setup and administration; assisting with centralised ethics and governance coordination; participant recruitment, screening and follow-up; data collection; database support; and assisting with project progress reporting.
The successful candidate will facilitate and maintain close working relationships with multidisciplinary clinical and research teams, clinicians, higher degree research students, participants and their parents, and other key stakeholders.
Key responsibilities will include, but are not limited to: In collaboration with the trial team, develop, promote and implement participant recruitment and engagement strategies and activities, including engaging with medical practitioners, sports clubs and schools; and adapt strategies as needed to meet recruitment targets.
Screen volunteers for suitability to enter the clinical trial according to study-specific inclusion/exclusion criteria.
Conduct informed consent procedures, enrol participants in the trial, and perform randomisation procedures.
Collect data (including questionnaires and study-specific assessments) from participants at scheduled timepoints, as described in the trial protocol.
Perform data entry, maintain systematic participant information record keeping, and assist with maintenance of project-specific clinical trial management systems.
Provide project administrative support to all stakeholders to develop a working framework and documentation for a multi-centre clinical trial, including preparing and presenting progress reports and study updates.
Assist with providing data for reporting on research outcomes, including preparation of abstracts, posters, oral presentations and publications.
About You The Clinical Trial Coordinator will be responsible for recruiting, screening and collecting data from adolescents with patellofemoral (kneecap) pain.
As such, our ideal candidate will be a health professional with the ability to diagnose musculoskeletal conditions within their scope of practice (e.g.
Physiotherapist, Podiatrist), have experience assessing and treating adolescents with musculoskeletal pain and injury, and have the following attributes:
Tertiary qualifications in health sciences (or other relevant disciplines), or experience and research management expertise in a tertiary setting; or an equivalent combination of relevant experience and/or education/training.
Ability to build relationships with a range of researchers, clinicians and other stakeholders, and work collaboratively as part of a multidisciplinary team in a co-operative and collegial manner.
Ability to effectively communicate with stakeholders at all levels (including adolescents), both internal and external to the organisation.
Excellent organisation skills, including the ability to prioritise workload and exercise initiative and judgement as appropriate.
Work in a flexible and dynamic environment with competing priorities to meet deadlines.
Well-developed skills in written communication, including flexibility and proficiency in using a wide range of computer and web applications to achieve high standard communication and promotional materials.
Knowledge of clinical research data capture and management using REDCap is desirable but not essential.
Mandatory Requirements: You must maintain unrestricted work rights in Australia for the duration of this appointment to apply.
Employer sponsored work rights are not available for this appointment.
The successful candidate will also be required to hold and maintain AHPRA registration, hold appropriate Working with Children clearance in Queensland (e.g.
Blue Card), and complete mandatory immunisations (as they apply to this position).
Applications close Monday 20 January 2025 at 11.00pm AEST (Job Reference Number: R-46605).
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