Medical Monitor
- Adelaide
- Salary:$150000 - $180000 per annum, Benefits: Great Salary Package
- Salary$150000 - $180000 per annum, Benefits: Great Salary Package
- LocationAdelaide
- Job type Full Time
- DisciplineClinical Research
- ReferenceBH-39289
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Medical Monitor
Job description
Benefits
About the company
Our client is a fast-growing CRO company. You will work across multiple therapeutic areas across all phases. Join a close kit team that emphasises support and valuing employee contribution.
About the opportunity
You will be an important member of the clinical project team. You will be responsible for providing medical and academic input cross functionally to the organisation ensuring high quality project delivery that aligns with internal objectives and budget requirements. You will liaise with investigators providing them information on the study, overseeing medical and safety aspects, while participating in data review and helping to ensure overall project success
Duties
Skills and Experience
Culture
Highly dynamic CRO that is expanding its presence in the APAC region. Join a fast growing and innovative company that awards hard work
How to Apply
Click apply or contact Maddy Rhodes–Laird, Senior Recruitment Consultant on 03 9938 7101 for a confidential discussion.
- Join a leading global CRO
- Work on wide range of trials across pharma and medical devices
- Great progression opportunities
About the company
Our client is a fast-growing CRO company. You will work across multiple therapeutic areas across all phases. Join a close kit team that emphasises support and valuing employee contribution.
About the opportunity
You will be an important member of the clinical project team. You will be responsible for providing medical and academic input cross functionally to the organisation ensuring high quality project delivery that aligns with internal objectives and budget requirements. You will liaise with investigators providing them information on the study, overseeing medical and safety aspects, while participating in data review and helping to ensure overall project success
Duties
- Provide medical and academic expertise
- Responsible for medical and safety monitoring of participants during the clinical trial
- Provide clinical input into the development and review of study protocols, procedure manuals, data collection tools and data quality plans
- Develop and provide protocol training
- Input into ongoing training and education materials for project investigators
- Provide support to the sites, resolving queries related to medical issues around patient eligibility, recruitment, treatment and management and adverse events
Skills and Experience
- Qualified medical doctor
- Experience working in a research institution or CRO
- Phase I experience
- Working knowledge of current ICH/GCP, ethical and regulatory requirements
- Strong communication skills – both written and verbal
- Exceptional organisational skills and attention to detail
- Flexible and adaptable
- Excellent problem-solving ability
Culture
Highly dynamic CRO that is expanding its presence in the APAC region. Join a fast growing and innovative company that awards hard work
How to Apply
Click apply or contact Maddy Rhodes–Laird, Senior Recruitment Consultant on 03 9938 7101 for a confidential discussion.