Clinical Data Specialist

Clinical Data Specialist RoleThis is a key position in our organization, requiring an individual to program listings and mappings, create visualizations, and review clinical data. The Clinical Data Specialist will also automate tasks, configure data extraction and transformations, and partner with stakeholders.Key Responsibilities:Program listings and...

Clinical Data Coordinator RoleAbout the PositionWe are seeking a skilled Clinical Data Coordinator to oversee data management activities for ongoing clinical studies.Key Responsibilities:Ensure timely, accurate, and complete data entry and validation.Perform data cleaning, query management, and discrepancy resolution.Prepare data reports, summaries, and...

Job TitleWe are seeking a Senior Clinical Data Coordinator to join our team at a leading organization. The successful candidate will be responsible for ensuring the accuracy and integrity of clinical trial data.Manage project-specific documents and CRFs in accordance with protocolsInitiate and manage DMTMF and e-filing processesPrepare project-specific...

Job Title: Clinical Data Configurator">Develop data specifications in compliance with SDTM, ADaM datasets and pooled analysis (ISS/ISE) standards.Design and validate analysis datasets, tables, listings, and figures for safety and efficacy parameters.Ensure adherence to ICH-GCP guidelines, core operating procedures, and work instructions.Maintain project...

Lab Data Analyst PositionThis position involves providing expert clinical lab data support to develop and maintain Laboratory Data Management tasks for studies awarded to our organization.The key responsibilities of this role include reviewing and processing large datasets, analyzing trends, and supporting the development of new systems and processes related...

Job Summary:We are seeking an experienced Senior Clinical Data Manager to oversee the clinical data management function. This role involves managing and ensuring that all data is accurate, complete, and compliant with regulatory requirements.The ideal candidate will have 10-15 years of experience in clinical trial/data management and data operations.

Job DescriptionAs a senior statistical programmer, you will be working with clinical trial data in the pharmaceutical and biotech industry. You will leverage your advanced SAS programming skills and proficiency in CDISC standards to support or lead one or more Phase I-IV clinical trials.

Seeking a meticulous Clinical Research Coordinator to assist in managing longitudinal clinical trials.The successful candidate will work closely with the research team, providing support for daily operations and coordinating participant activities, including Continuous Glucose Monitoring (CGM) setup, lab tests, gut microbiome analysis, and remote...

Job Opportunity: Central Data Integrity SpecialistThe role of the Central Monitor II plays a pivotal part in maintaining data quality and integrity through comprehensive monitoring activities, statistical review, and proactive risk management.Key Responsibilities:Conduct thorough risk assessments for clinical studies, identifying potential issues and...

Job Overview:This position is responsible for designing, building, and operating scalable data pipelines to process clinical encounter data and integrate healthcare information. The ideal candidate will collaborate closely with software engineers, machine learning specialists, and clinical partners to drive project success.Key Responsibilities:Design...