Clinical Trial Manager II
3 weeks ago
As a Clinical Trial Manager II, you will be part of a dynamic team responsible for managing clinical trials from start to finish. Your primary focus will be on ensuring the successful execution of clinical trials, meeting quality and regulatory requirements, and delivering high-quality data to our clients.
Key Responsibilities:- Study Management: Manage and prioritize clinical deliverables to ensure timely completion, quality, and regulatory compliance.
- Team Leadership: Lead and motivate a team of clinical professionals, providing guidance, training, and performance feedback to ensure high-quality results.
- Risk Management: Identify and mitigate potential risks within study protocols and operational aspects of trials.
- Quality Assurance: Ensure quality standards and regulatory requirements are met, collaborating with quality assurance department members to identify and address any issues.
- Communication: Effectively communicate with sponsors, project managers, functional team leads, and other project team members to ensure seamless collaboration and information exchange.
- Education: Bachelor's degree in a health, life sciences, or relevant field of study.
- Experience: 8 years of relevant experience in clinical research or a related field.
- Skills: Advanced project management skills, excellent leadership and influencing skills, and high proficiency with Microsoft Office and company collaboration applications.
At ICON, we value diversity, inclusion, and belonging. We offer a competitive salary, a range of benefits, and opportunities for professional growth and development. Our benefits include various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
We are committed to providing an inclusive and accessible environment for all candidates. If you need a reasonable accommodation for any part of the application process, please let us know. We look forward to hearing from you
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Clinical Trial Manager II
2 weeks ago
Darwin, Northern Territory, Australia Pharmiweb Full timeJob Title: Clinical Trial Manager IIAs a Clinical Trial Manager II, you will be responsible for managing and prioritizing clinical deliverables to ensure quality and regulatory requirements are met. You will work closely with cross-functional teams to achieve successful delivery of data.Key Responsibilities:Manage and prioritize clinical deliverables to...
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Clinical Trial Manager II
3 weeks ago
Darwin, Northern Territory, Australia Pharmiweb Full timeJob Title: Clinical Trial Manager IIAs a Clinical Trial Manager II, you will be part of a dynamic team at ICON, a leading global provider of clinical research services. We are seeking an experienced professional to manage and prioritize clinical deliverables, ensuring quality and regulatory requirements are met.Key Responsibilities:Manage and prioritize...
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Clinical Research Associate II Specialist
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Clinical Research Associate II Specialist
2 days ago
Darwin, Northern Territory, Australia Pharmiweb Full timeJob SummaryWe are seeking a Clinical Research Associate II Specialist to join our team. 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 ResponsibilitiesConduct site...
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Clinical Research Associate II Specialist
2 days ago
Darwin, Northern Territory, Australia Pharmiweb Full timeJob SummaryWe are seeking a 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
2 weeks ago
Darwin, Northern Territory, Australia Pharmiweb Full timeJob Title: Clinical Research Associate IIAs a Clinical Research Associate II at Pharmiweb, you will be part of a dynamic team responsible for the successful execution of clinical trials. Your primary responsibilities will include assessing the qualifications of potential clinical study sites, implementing clinical studies at participating sites, managing the...
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