Clinical Trials Data Insight Specialist

Clinical Trial Data Analyst Job DescriptionLabcorp is seeking a skilled Clinical Trial Data Analyst to join our team. As a Clinical Trial Data Analyst, you will be responsible for ensuring the accuracy and integrity of clinical trial data. This includes analyzing data, identifying trends, and making recommendations for improvement.Key...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in a key role within our global clinical trials organization. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice guidelines.Key...

Job Title: Clinical Research Associate - Oncology Trials SpecialistAs a Clinical Research Associate - Oncology Trials Specialist, you will be responsible for working on multiple trials within Oncology, focusing on start-up activities. Your primary goal will be to collaborate with country operations teams to identify, select, and activate clinical trial sites...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in a key role within our Oncology Trials department. As a Clinical Research Associate, you will be responsible for managing clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to deliver high-quality results.Key...

Job Summary:We are seeking a 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 Responsibilities:Conduct...

Key Responsibilities:Essential Criteria:1. Identify organisational challenges and problem statements, and translate them into analytical and data business requirements.2. Articulate complex information into simple messages for key stakeholders with varied levels of data literacy.3. Design and build reports, dashboards, and data products that support business...

Clinical Data Risk Analyst Job DescriptionWe are seeking a highly skilled Clinical Data Risk Analyst to join our team at ICON plc. As a Clinical Data Risk Analyst, you will be responsible for set-up and implementation of Central Monitoring on a portfolio of clinical studies.Key Responsibilities:Recognize, exemplify and adhere to ICON's values, which center...

Clinical Data Risk Analyst Job DescriptionWe are seeking a skilled Clinical Data Risk Analyst to join our team at ICON plc. As a Clinical Data Risk Analyst, you will be responsible for set-up and implementation of Central Monitoring on a portfolio of clinical studies. This is an exciting opportunity to work with a world-leading healthcare intelligence and...

Clinical Research Associate RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Pharmiweb. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.Key Responsibilities:Site Qualification and Monitoring: Conduct site qualification, initiation, monitoring, and close-out visits for...

Company OverviewAt Research at Icon Group, we are committed to providing exceptional cancer care services. With a growing reach into New Zealand and Asia, our company has over 3,500 employees company-wide.We have more than half of our locations participating in clinical trials, making us Australia's largest private cancer clinical trials program.About the...

About the RoleWe are seeking a highly skilled and motivated Clinical Research Coordinator to join our team at Icon Research. As a key member of our research team, you will be responsible for coordinating and conducting clinical trials, ensuring that all research activities are conducted in accordance with Good Clinical Practice and Icon policies.Key...

Clinical Research Coordinator Role SummaryWe are seeking a highly skilled and motivated Clinical Research Coordinator to join our research team at Icon Group. As a key member of our team, you will play a crucial role in the conduct and day-to-day management of clinical trials. Your primary responsibility will be to provide high-level support to our Principal...

About the RoleWe are seeking a highly skilled and motivated Clinical Research Coordinator to join our team at Research at Icon Group. As a key member of our research team, you will be responsible for coordinating and conducting clinical trials, ensuring compliance with Good Clinical Practice and Icon policies.Key Responsibilities:Provide high-level support...

Job DescriptionWe are seeking a highly skilled Clinical Site Manager to join our team at Pharmiweb. As a Clinical Site Manager, you will be responsible for managing clinical trials at various sites, ensuring compliance with regulatory requirements and Good Clinical Practices (GCP).Key Responsibilities:Develop and implement site engagement strategies to...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team in the pharmaceutical industry. As a Clinical Research Associate, you will be responsible for monitoring pharmaceutical industry clinical trials, ensuring compliance with regulatory requirements, and providing high-quality support to our clients.Key...

Senior Auditor, Quality Assurance SpecialistWe are seeking a Senior Auditor, Quality Assurance Specialist to join our team at ICON. In this role, you will play a pivotal part in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key...

Job SummaryAs a Senior Clinical Research Associate at Pharmiweb, you will play a critical role in the success of our clinical trials. Your primary responsibility will be to ensure the smooth execution of clinical studies, from site qualification to close-out. You will work closely with cross-functional teams to identify and mitigate risks, and develop...

Job DescriptionWe are seeking a highly skilled Clinical Research Associate II to join our team at Pharmiweb. As a Clinical Research Associate II, you will be responsible for assessing the qualifications of potential clinical study sites, implementing clinical studies at participating sites, managing the conduct of clinical studies at sites, ensuring the...

Parexel Job OpportunityOur company is looking for a highly skilled Statistical Programmer to support various SAS programming activities related to the analysis and reporting of clinical study data. As a Statistical Programmer, you will use programming techniques to produce analysis datasets, tables, figures, and data listings, ensuring first-time quality,...

Role OverviewWe are seeking a highly skilled Clinical Specialist to join our team at JPS Medical Recruitment. As a key member of our Acute Care Team, you will be responsible for providing expert care to patients in a fast-paced and dynamic environment.Key ResponsibilitiesProvide specialist care to patients in the acute care settingWork collaboratively with...