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Clinical Data Management
Katalyst Healthcares and Life SciencesBoston, MA, United StatesScientist I, Data Management
Foundation Medicine400 Summer Street, Boston, Massachusetts, US- Promoted
Associate Director Data Analysis & Management
Dana-Farber Cancer InstituteBoston, MA, United States- Promoted
Director of Product Management, Data Analytics
OUTFRONT Media LLCBoston, MAManager, Clinical Data Management
IntePros ConsultingCambridge, Massachusetts, USData Management Platform Manager
Mass General BrighamSomerville, Massachusetts, US- Promoted
Clinical Data Management
Katalyst HealthCares & Life SciencesCambridge, MA- Promoted
Data Management Job Training Opportunity
Year Up United CareersMalden, MA, United States- Promoted
Senior Director, External Data Management
Sarepta TherapeuticsCambridge, MA, United States- Promoted
Associate Director of Clinical Data Management
Alira HealthBoston, MA, United States- Promoted
Director, Technical Program Management - Enterprise Data
Capital OneCambridge, MA, United StatesManager, Data Management
PROMETRIKA, LLCCAMBRIDGE ,MA, Cambridge, MA, USSecurities Data Management Analyst
MassMutualBoston, Massachusetts, US- Promoted
RDQ Data Management and Governance Leader
TakedaCambridge, Massachusetts, United States- Promoted
Cybersecurity and Data Management Senior Counsel
Bain & CompanyBoston, MAData Management Contract Lead
The Judge GroupCambridge, MAData Management Platform Manager
Partners HealthCareSomerville, MA, USClinical Data Management
Katalyst Healthcares and Life SciencesBoston, MA, United States- Full-time
Responsibilities : Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies. Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules. Ensure proper completion of QC and UAT of EDC tools and modules, including database testing, data export testing, and testing of custom programming. Coordinate with Sponsor and Vendors to ensure efficiency and quality of electronic data receipt, integration, and reconciliation. Design "smart " listings and study-specific processes for effective data review, query issue and resolution. Perform coding of adverse events, medical conditions and medications. Perform SAE reconciliation. Lead and perform pre-lock and data lock tasks. Prepare training materials and user guides for EDC data collection tools, deliver user training. Design, generate, and review status metric reports, identifying and communication trends as needed. Provide input to cross-functional study timelines and resource requirements to ensure timely completion of project milestones for complex studies. Provide study specific training for team members and end users, as appropriate. Lead large and complex projects. Lead client and team meetings as required. Interact with sponsors and manage vendors for complex studies. Present at sales and marketing meetings for prospective clients. Develop SOPs and manuals. Requirements : Minimum 9 years of experience in Clinical Data Management. Minimum BS in a scientific or health related field or equivalent. Previous experience working for a CRO required. Knowledge of medical terminology and pharmaceutical notation. Expertise with EDC systems, such as Medidata Rave, InForm, Medrio. Excellent organizational and time management skills. Strong collaboration and leadership skills .