About the Role 

Join our team as a Clinical Research Coordinator on a 0.6FTE, fixed term (ending Dec 2028) to work at MCHRI based at Clayton.The Clinical Research Coordinator will provide research and administrative support to the iIMPROVE group at Monash Emergency Research Collaborative (MERC), working closely with senior research staff to support the delivery of clinical research projects within the implementation science framework. The role will contribute to study coordination, data management, ethics and governance activities, and communication with internal and external collaborators. The appointee will work with support, guidance and direction from the Senior Project Manager, iIMPROVE and the iIMPROVE team. This is an opportunity for a highly organised individual with strong attention to detail and an interest in clinical and/or implementation science research to contribute to impactful research outcomes.  

• Provide administrative support across clinical research activities, including ethics and governance submissions, study documentation and project coordination  
• Support participant recruitment, research visits, study monitoring and data verification activities 
• Assist investigators in day-to-day conduct of multiple concurrent studies. 
• Preparation and maintenance of study documents including maintaining source documents, Investigator Site Files and Trial Master Files. 
• Respond to data queries and ensure documentation is audit ready. 
• Ensuring studies are conducted in accordance with regulatory and ethical guidelines as well as Ethics approved protocols and funder reporting requirements. 
• Prepare manuscripts drafts with investigators 
• Submit papers for peer review 

Hybrid working arrangement is offered. 

About You  

To be successful in this healthcare role, you will bring the following demonstrated skills, experience, and attributes. 

Essential:

• Demonstrated skills in the coordination of data collection, data entry and analysis using Excel. 
• Experience in working with computer based data acquisition and analysis systems. 
• Experience in working with management of large and complex datasets equivalent to post graduate (honours) study or higher. 
• Excellent interpersonal skills and demonstrated ability to work effectively as a member of an interdisciplinary team, including the ability to liaise and negotiate with research, clinical and nursing staff. 
• Demonstrated organisational skills including the demonstrated ability to maintain a high standard of data record keeping and a demonstrated ability to meet competing deadlines. 
• Excellent oral, written communication and presentation skills. 
• Ability to establish and maintain constructive working relationships with stakeholders both internal and external to the emergency network. 
• Experience in negotiating with multiple organisations and professional groups within a project management framework. 
• A commitment to confidentiality, total discretion and integrity. 

Desirable:

• Experience in the operations and administration of multi-centre clinical research. 
• Experience in data collection and with using SPSS 
• Experience and demonstrated skill using information technology systems applicable to research, e.g. cloud based data sharing, surveys platforms, and file transfer protocols.  

Why you will love working with us  

Ours is a connected team with strong shared values and an unwavering commitment to excellence. We are a highly skilled, collaborative, and welcoming team where the only limit in your career is you. Upon your appointment, we will provide you with:

• A supportive and cohesive sub-team, working within a larger consumer relations team.  
• Professional development courses, seminars and mentoring.  
• Opportunities for you to use your experience in the role to inform and drive initiatives within the broader units and programs.  
• Salary packaging.  
• Onsite Gym options and ability to join Fitness Passport - your pass to an extensive choice of fitness facilities.  

For a confidential discussion and to explore this opportunity further, please reach out to Komal Daredia, Senior Project Manager by email at komal.daredia@monash.edu.

Position Description can be found here

Our Culture and Values 

At Monash Health, our people are at the heart of everything we do. Our culture is inclusive, supportive and future-focused, underpinned by clear values and a commitment to continuous improvement. 

Our teams play a critical role in bringing our new strategy to life, challenging traditional approaches, embracing innovation, and ensuring every appointment reflects our commitment to equity, transparency and excellence. 

You’ll be encouraged to share ideas, contribute to improvement initiatives, and grow alongside experienced professionals who are passionate about what they do. 

We are Full Hearted, Open Minded and All In, enabling excellent service delivery and a positive candidate and employee experience every time. 

We recognise the value of equal employment opportunity. We are committed to patient safety, promoting fairness, equity and diversity in the workplace and to Child Safe Standards.

About the Role 

Join our team as a Clinical Research Coordinator on a 0.6FTE, fixed term (ending Dec 2028) to work at MCHRI based at Clayton.The Clinical Research Coordinator will provide research and administrative support to the iIMPROVE group at Monash Emergency Research Collaborative (MERC), working closely with senior research staff to support the delivery of clinical research projects within the implementation science framework. The role will contribute to study coordination, data management, ethics and governance activities, and communication with internal and external collaborators. The appointee will work with support, guidance and direction from the Senior Project Manager, iIMPROVE and the iIMPROVE team. This is an opportunity for a highly organised individual with strong attention to detail and an interest in clinical and/or implementation science research to contribute to impactful research outcomes.  

• Provide administrative support across clinical research activities, including ethics and governance submissions, study documentation and project coordination  
• Support participant recruitment, research visits, study monitoring and data verification activities 
• Assist investigators in day-to-day conduct of multiple concurrent studies. 
• Preparation and maintenance of study documents including maintaining source documents, Investigator Site Files and Trial Master Files. 
• Respond to data queries and ensure documentation is audit ready. 
• Ensuring studies are conducted in accordance with regulatory and ethical guidelines as well as Ethics approved protocols and funder reporting requirements. 
• Prepare manuscripts drafts with investigators 
• Submit papers for peer review 

Hybrid working arrangement is offered. 

About You  

To be successful in this healthcare role, you will bring the following demonstrated skills, experience, and attributes. 

Essential:

• Demonstrated skills in the coordination of data collection, data entry and analysis using Excel. 
• Experience in working with computer based data acquisition and analysis systems. 
• Experience in working with management of large and complex datasets equivalent to post graduate (honours) study or higher. 
• Excellent interpersonal skills and demonstrated ability to work effectively as a member of an interdisciplinary team, including the ability to liaise and negotiate with research, clinical and nursing staff. 
• Demonstrated organisational skills including the demonstrated ability to maintain a high standard of data record keeping and a demonstrated ability to meet competing deadlines. 
• Excellent oral, written communication and presentation skills. 
• Ability to establish and maintain constructive working relationships with stakeholders both internal and external to the emergency network. 
• Experience in negotiating with multiple organisations and professional groups within a project management framework. 
• A commitment to confidentiality, total discretion and integrity. 

Desirable:

• Experience in the operations and administration of multi-centre clinical research. 
• Experience in data collection and with using SPSS 
• Experience and demonstrated skill using information technology systems applicable to research, e.g. cloud based data sharing, surveys platforms, and file transfer protocols.  

Why you will love working with us  

Ours is a connected team with strong shared values and an unwavering commitment to excellence. We are a highly skilled, collaborative, and welcoming team where the only limit in your career is you. Upon your appointment, we will provide you with:

• A supportive and cohesive sub-team, working within a larger consumer relations team.  
• Professional development courses, seminars and mentoring.  
• Opportunities for you to use your experience in the role to inform and drive initiatives within the broader units and programs.  
• Salary packaging.  
• Onsite Gym options and ability to join Fitness Passport - your pass to an extensive choice of fitness facilities.  

For a confidential discussion and to explore this opportunity further, please reach out to Komal Daredia, Senior Project Manager by email at komal.daredia@monash.edu.

Position Description can be found here

Our Culture and Values 

At Monash Health, our people are at the heart of everything we do. Our culture is inclusive, supportive and future-focused, underpinned by clear values and a commitment to continuous improvement. 

Our teams play a critical role in bringing our new strategy to life, challenging traditional approaches, embracing innovation, and ensuring every appointment reflects our commitment to equity, transparency and excellence. 

You’ll be encouraged to share ideas, contribute to improvement initiatives, and grow alongside experienced professionals who are passionate about what they do. 

We are Full Hearted, Open Minded and All In, enabling excellent service delivery and a positive candidate and employee experience every time. 

We recognise the value of equal employment opportunity. We are committed to patient safety, promoting fairness, equity and diversity in the workplace and to Child Safe Standards.