Katalyst Data Management

60 Katalyst Data Management Jobs Hiring Near You

Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines * Oversee data cleaning activities, including the generation, review, and resolution ...

Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized ...

Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. * Oversee data cleaning activities, including the generation, review, and resolution ...

Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized ...

Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized ...

Regularly monitor data management costs of the assigned studies ensuring respect of budget. * Define and proactively manage risks with potential impact on study systems setup, study conduction, or ...

Regularly monitor data management costs of the assigned studies ensuring respect of budget. * Define and proactively manage risks with potential impact on study systems setup, study conduction, or ...

In this pivotal role, you will oversee the collection, management, and validation of clinical trial data to ensure accuracy, integrity, and compliance with regulatory standards. Your expertise will ...

In this pivotal role, you will oversee the collection, management, and validation of clinical trial data to ensure accuracy, integrity, and compliance with regulatory standards. Your expertise will ...

Responsible for the oversight of all data management CRO activities supporting company's clinical programs from database start-up through database lock and CSR/submission. * Serves as primary point ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Oversee data management activities to maintain consistency across trials including Case Report Form (CRF) design, Data Management Plans, CRF annotation, edit check programs, data entry and query ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks. * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC build and associated edit checks * Provide study level metrics/reports and external data reconciliation ...

Showing results 41-60

Katalyst Data Management Jobs Information

Infographic showing various job openings at Katalyst Data Management in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.
Clinical Data Manager

Other

Posted 22 days ago


Job description

Responsibilities:
  • The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock
  • The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements
  • This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution
  • Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol
  • Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines
  • Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams
  • Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations
  • Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP)
  • Manage database lock activities and contribute to the preparation of clinical study reports (CSRs)
  • Serve as the primary point of contact for data management vendors and oversee their deliverables
  • Participate in study team meetings and provide status updates related to data quality and timelines
  • Support audit readiness and participate in regulatory inspections when required
Requirements:
  • Bachelor's degree in Life Sciences, Computer Science, Health Informatics, or related field
  • Minimum of 3-5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment
  • Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap)
  • Strong understanding of ICH-GCP, FDA regulations, and CDISC standards
  • Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug)
  • Excellent organizational, analytical, and problem-solving skills
  • Strong communication and collaboration skills across cross-functional teams