Trial Coordinator

**Job no**: 528579
**Work type**: Part Time
**Location**: Sydney, NSW
**Categories**: Clinical/Medical Research
- **One of Australia’s leading research & teaching universities**:

- **Vibrant campus life with a strong sense of community & inclusion**:

- **Enjoy a career that makes a difference by collaborating & learning from the best**

**At UNSW, we pride ourselves on being a workplace where the best people come to do their best work.**

The Trial Coordinator supports the activities of a Medical Research Future Fund (MRFF) funded randomised controlled trial. Led by Professor Anstey, this project aims to reduce the risk factors for late life dementia in older adults who experience Subjective Cognitive Decline (SCD) or Mild Cognitive Impairment (MCI).

**About the role**
- **LEVEL 6 ($100k - $107k)** plus 17% Superannuation and annual leave loading
- Fixed Term - 2 years
- Part time (21 hours)

The role reports to Professor Kaarin Anstey, supporting the Faculty of Science and School of Psychology and has no direct reports.

**Specific responsibilities for this role include**:

- Provision of practical and efficient research support to stakeholders, assisting in the conduct of an online randomised controlled trial of dementia risk reduction interventions for individuals with Subjective Cognitive Decline (SCD) and Mild Cognitive Impairment (MCI).
- Prepare, contribute, and manage participant communications, project team meetings, reports in relation to study progress and timeline.
- Oversee data management and storage in line with Good Clinical Practice ensuring integrity in research databases, quality control and ethical standards.
- Perform quantitative/qualitative data analyses as required by the research project.
- Monitor research protocols, provide problem solving and resolution to any evolving problems related to design, implementation, and analysis.
- Liaise with organisations, stakeholders and collaborators and actively participate in meetings and discussions as required.
- Coordinate, plan and complete day-to-day research activities within the framework of agreed project timelines and responsibilities.
- Assist with transferring biospecimens between facilities where required and according to protocols.
- Assist with accurately and securely onboarding participants including obtaining informed consent, eligibility screening, appointment scheduling, session debriefs and managing participant wellbeing
- Assist with participant communication, coordinate incidental reporting from pathology collaborators and manage highly sensitive data.
- Align with and actively demonstrate the Code of Conduct and Values.
- Cooperate with all health and safety policy and procedures of the University and take all reasonable care to ensure your actions or omissions do not impact on the health and safety of yourself and others.

**About the successful applicant**
**(Selection Criteria)**

To be successful in this role you will have:

- A tertiary degree in Psychology or a related field (Bachelor’s degree with Honours or Master’s degree) or an equivalent level of knowledge gained through a combination of education, training or experience.
- Knowledge of human research ethics, clinical research practices, ICH/Good Clinical Practice, and data privacy and handling highly sensitive data.
- Experience in supporting the conduct of human clinical trials and an understanding of research protocols, design, planning and experimental methods.
- Experience in participant recruitment, survey design, implementation, data collection and data management.
- Demonstrated superior interpersonal communication skills to initiate and maintain effective stakeholder relationships whilst exercising discretion and confidentiality.
- Excellent time management skills, with a demonstrated ability to respond to changing priorities, manage multiple tasks and meet competing deadlines by using judgement and initiative.
- Excellent written and verbal communication skills, with a high level of attention to detail and the ability to liaise effectively with a range of stakeholders.
- Demonstrated ability to work collaboratively and productively within a team, but also to take initiative and work independently while managing competing demands.
- Demonstrated interest in cognitive ageing, epidemiology, and dementia.
- Demonstrated ability to adhere to standard protocols, clinical reporting obligations and safety requirements.
- An understanding of and commitment to UNSW’s aims, objectives, and values in action, together with relevant policies and guidelines.
- Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training.

**Contact**:
Ranmalee Eramudugolla
**Applications close**: November 26th, 2024
- UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ+ community; an