Clinical Trial Coordinator

About the OpportunityThis Senior Clinical Trial Coordinator role offers an exciting opportunity to work on innovative projects at the forefront of the industry. As a key member of the global biometrics delivery team, you will be responsible for providing overall leadership and management for database programming, data integration, data management, and...

About the PositionWe are seeking a highly skilled Clinical Data Coder to join our IQVIA LLC team.The successful candidate will be responsible for managing single and multi-service projects, ensuring quality deliverables on time and to customer satisfaction.Key Responsibilities:Serve as an account lead for standalone coding studies or accounts.Manage the...

Job Overview:IQVIA's Global Site Activation Team is a global network that identifies and activates sites to the highest quality to ensure patients on clinical trials have access to safe and effective medication.You will review documents for completeness, consistency, and accuracy, under the guidance of senior staff. You will also prepare site regulatory...

Job RequirementsWe are looking for a professional with 1-3 years of experience in data management for the base level and more than 3 years of experience for the advanced level.The ideal candidate will have project management skills and vendor management skills. They should also be able to interpret clinical trial data and present trends to clinical trial...

Job DescriptionWe are seeking a highly skilled Senior Clinical Trials Manager to join our team. In this role, you will be responsible for leading clinical trials, developing project plans, and managing multiple projects simultaneously.About the JobYou will lead cross-functional teams, including project managers, researchers, and other stakeholders.You will...

At IQVIA, we are committed to improving patients' lives by bringing new drugs to the market faster. As a Clinical Lead for Oncology Trials, you will play a key role in leading and working alongside clinical teams to deliver large, global trials.The Clinical Lead is responsible for ensuring clinical delivery of assigned projects in compliance with regulatory...

Key ResponsibilitiesOversee the management of clinical trials, providing data management support, oversight and/or accountability.Work with trial customers and other internal and external partners to establish, align and confirm data management expectations.Create, plan and track content, format, quality and timing of data management deliverables.Perform...

Your ResponsibilitiesA minimum of 2+ years of relevant operational clinical trial management experience is required. You should have expertise in the use of study and site dashboards and reporting tools, as well as experience in study start-up.

Job SummaryAs a Senior Clinical Lead in our Oncology delivery unit, you will be responsible for leading and working alongside clinical teams to deliver large, global trials. You will contribute to the development of the project risk mitigation plan and manage clinical risks through the project lifecycle.Key ResponsibilitiesEnsure clinical delivery of...

Job DescriptionCreate SAS programs to generate derived analysis datasets and content for tables, listings, and figures;Perform programming validation to ensure quality of analysis datasets and programming outputs.The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in...

Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up, Execution,...

Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up, Execution,...

Clinical Data Associates are integral to the success of clinical trials at IQVIA LLC. As a Clinical Data Associate, you will play a critical role in ensuring the integrity and quality of clinical data.Key Responsibilities:Data Review and Query GenerationData Reconciliation and ValidationStudy Meetings and TeleconferencesStudy Closeout and Archiving...

When our values align, there's no limit to what we can achieve.Parexel is currently seeking a Clinical Programmer to join us in South Africa, dedicated to a single sponsor.This role will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups...

Job OverviewIQVIA Argentina is seeking a skilled Clinical Data Management Lead to oversee the management of clinical trials.This role involves providing data management support, oversight and/or accountability for one or more clinical trials. The successful candidate will take the lead with trial customers and other internal and external partners to...

Parexel is a leading clinical research organization that supports studies across various therapeutic areas. As a Clinical Programmer, you will be part of our team dedicated to delivering high-quality data review and trial management services.This role requires the provision of data review and trial management deliverables for multiple compounds and trials....

Looking for a data management expert who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).Prior experience of closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when...

Looking for a data management expert, who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).Prior experience of closely collaborating with the SRP, SRS, Data Management functions, and the rest of the study team members when...

Clinical Data Associates at IQVIA LLC are responsible for ensuring the integrity and quality of clinical data. Key responsibilities include data review, query generation, data reconciliation, and study closeout activities.Required Skills and Qualifications:Bachelor's degree in a Health or Science discipline with experience in clinical research.Data...

Job DescriptionIQVIA Argentina is seeking a Senior Clinical Research Associate to join our team. The ideal candidate will have extensive experience in clinical research and a proven track record of conducting monitoring and site management work.The role involves conducting site visits, adapting and driving subject recruitment plans, and administering...