Clinical Research Associate II Specialist
4 days ago
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be a part of our mission to shape the future of clinical development.
Key Responsibilities:
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits, including various annual leave entitlements, a range of health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme.
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Clinical Research Associate II Specialist
5 days ago
Melbourne, Victoria, Australia Pharmiweb Full timeJob SummaryWe are seeking a highly skilled Clinical Research Associate II Specialist to join our team at ICON. As a Clinical Research Associate II Specialist, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key...
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Clinical Research Associate II Specialist
1 month ago
Melbourne, Victoria, Australia Pharmiweb Full timeClinical Research Associate II SpecialistWe are seeking a highly skilled and motivated Clinical Research Associate II Specialist to contribute to the advancement of innovative treatments and therapies at ICON plc, a world-leading healthcare intelligence and clinical research organization.Key Responsibilities:Conduct site qualification, initiation,...
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Clinical Research Associate II Specialist
1 month ago
Melbourne, Victoria, Australia Pharmiweb Full timeClinical Research Associate II SpecialistWe are seeking a highly skilled and motivated Clinical Research Associate II Specialist to contribute to the advancement of innovative treatments and therapies. As a key member of our diverse and dynamic team, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data,...
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Clinical Research Associate II Specialist
3 weeks ago
Melbourne, Victoria, Australia Pharmiweb Full timeClinical Research Associate II SpecialistICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.Key Responsibilities:Conduct site qualification, initiation,...
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Clinical Research Associate II
4 weeks ago
Melbourne, Victoria, Australia Pharmiweb Full timeAbout the RoleWe are seeking a highly skilled and experienced Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for conducting clinical trials and ensuring compliance with regulatory requirements.Key ResponsibilitiesConduct site qualification, site initiation, interim monitoring, site management...
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Clinical Research Associate II
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Melbourne, Victoria, Australia Pharmiweb Full timeJob SummaryPharmiweb is seeking a highly skilled Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.Key Responsibilities...
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