Description:
We've partnered with the global 'Top 3' global CRO looking to build their contractor team in Australia. They work on some of the leading clinical trials worldwide and have won several new project sin recent months. This is an initial 6 month contract but likely to be extended into years.
Regional travel to the city you are located in!
Key Responsibilities:
- The Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Standard Operating Procedures
- Conducts site visits to assess protocol and regulatory compliance and manages required documentation responsible for ensuring that data will pass international quality assurance audits
- Represents the client in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel
- May assist project manager or clinical team manager on assigned projects. Required to travel 60-80% on average
Education and Experience
- University degree in a science related field or a certified health care professional
- Previous experience as a clinical research monitor
- Valid Driver's License
- Knowledge, Skills and Abilities: Effective clinical monitoring skills
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures
- Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software
- Good English language and grammar skills Good presentation skills