Job details
- Location
- Brisbane
- Salary
- Competitive
- Job Type
- Full Time
- Ref
- BH-36951-1
- Contact
- Mattias Fitzgerald
- Posted
- over 1 year ago
Job details
- Location
- Brisbane
- Salary
- Competitive
- Job Type
- Full Time
- Ref
- BH-36951-1
- Contact
- Mattias Fitzgerald
- Posted
- over 1 year ago
Overview:
• Work for a multinational CRO company
• Take ownership of all site activities from initiation through to close-out
• Work with a single sponsor on an FSP model
Benefits:
• Excellent training and development opportunities
• Attractive salary package plus car allowance
• Flexible working arrangements - Home / Office based
About the company:
Working for a full service CRO that is an industry leader in providing world class solutions in pharmaceuticals and medical devices. Spanning across many therapeutic areas, this company focuses on quality and efficiency for client success. Join an inclusive team that emphasises building a professional network, investing in employees and fostering a close-knit team culture.
About the Opportunity:
The CRA is responsible for the preparation, initiation, monitoring and closure of an agreed number of centres in clinical studies according to procedural documents, international guidelines such as ICH and GCP as well as relevant local regulations. Deliver according to the commitment in the individual trials.
Duties:
• Ensures timelines are met from start up to closeout
• 30-60% non-local, national travel
• Monitoring sites and completing reports in timely manner
• Maintaining clear lines of communication with sites
• Providing protocol and related study training to assigned sites
• Manages site performance and collaborate to complete regulatory submissions & recruitment plans
Skills and Experience:
• Must have Australian independent monitoring experience of at least 12 months
• Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
• Preferred experience in monitoring Oncology or Autoimmune disease studies
• Reasonable understanding of Clinical Study Management including monitoring, study drug handling and data management
• AU working rights
Culture:
As a world renowned CRO, the company prides itself on leveraging connectivity and data driven solutions to drive success and encourages inclusion and diversity.
How to Apply:
Click apply or for a confidential discussion contact:
Mattias Fitzgerald, Recruitment Consultant on +61 2 8877 8749; or
Davina Ocansey, Senior Recruitment Consultant on +61 2 8877 8712
• Work for a multinational CRO company
• Take ownership of all site activities from initiation through to close-out
• Work with a single sponsor on an FSP model
Benefits:
• Excellent training and development opportunities
• Attractive salary package plus car allowance
• Flexible working arrangements - Home / Office based
About the company:
Working for a full service CRO that is an industry leader in providing world class solutions in pharmaceuticals and medical devices. Spanning across many therapeutic areas, this company focuses on quality and efficiency for client success. Join an inclusive team that emphasises building a professional network, investing in employees and fostering a close-knit team culture.
About the Opportunity:
The CRA is responsible for the preparation, initiation, monitoring and closure of an agreed number of centres in clinical studies according to procedural documents, international guidelines such as ICH and GCP as well as relevant local regulations. Deliver according to the commitment in the individual trials.
Duties:
• Ensures timelines are met from start up to closeout
• 30-60% non-local, national travel
• Monitoring sites and completing reports in timely manner
• Maintaining clear lines of communication with sites
• Providing protocol and related study training to assigned sites
• Manages site performance and collaborate to complete regulatory submissions & recruitment plans
Skills and Experience:
• Must have Australian independent monitoring experience of at least 12 months
• Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
• Preferred experience in monitoring Oncology or Autoimmune disease studies
• Reasonable understanding of Clinical Study Management including monitoring, study drug handling and data management
• AU working rights
Culture:
As a world renowned CRO, the company prides itself on leveraging connectivity and data driven solutions to drive success and encourages inclusion and diversity.
How to Apply:
Click apply or for a confidential discussion contact:
Mattias Fitzgerald, Recruitment Consultant on +61 2 8877 8749; or
Davina Ocansey, Senior Recruitment Consultant on +61 2 8877 8712
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