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Clinical Research Associate
2 months ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life. We are seeking a highly skilled Clinical Research Associate to join our team in Sydney, Australia.
The successful candidate will be responsible for monitoring and study management for Abbott clinical trials in Australia and New Zealand. This role will involve working closely with study site staff and Abbott Australia to ensure the successful execution of clinical trials.
Key Responsibilities- Assist in the identification and selection of investigators for clinical studies.
- Collect and maintain regulatory documentation, including ICH GCP/ISO 14155 guidelines.
- Participate in investigator meetings and conduct site assessment and initiation visits.
- Ensure protocol compliance and accurate data collection through source document verification.
- Liaise with key study personnel at Abbott's Headquarters and/or country offices.
- Assist in the preparation of monthly tracking reports for project management.
Requirements
- Nursing or biological science qualification, or equivalent combination of education and work experience.
- Preferably greater than 12 months experience in clinical studies working at a high level of competency.
- Good working knowledge of ICH GCP/ISO 14155 guidelines and other regulatory guidelines relevant to clinical research in Australia.
Abbott is committed to building a diverse workforce that values diversity across gender, age, culture, disability, and lifestyle.
In order to be eligible to work for Abbott in Australia or New Zealand, you must hold current working rights with no restrictions for the respective country applicable.
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