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The Sr Business Analyst (BA), Master Data Management (MDM) acts as an intermediary between the business and technical community. The Sr BA will work with IT project teams and business clients within all areas of the master data community to collect, clarify, and translate business requirements into documentation.
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Owns the Trial Master File for assigned trials; ensures appropriate quality oversight and QC of required elements of TMF. Owns the Trial Master File for assigned trials; ensures appropriate quality oversight and QC of required elements of TMF.
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Used as a developmental role, you will learn to master knife skills, fundamentals of rolling sushi and food safety. The Sushi Chef’s responsibilities include preparing traditional Japanese sushi rice, chopping, slicing and filleting various kinds of fish and maintaining a clean and safe work environment.
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Identifies and supports the DSPV team with document management activities (e.g., electronic Trial Master File, Veeva) 2+ years of experience in a pharmaceutical industry setting within Drug safety, Pharmacovigilance, or the equivalent.
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Active Electrical Journeyman’s (Class B) or Master Electrician (Class A) license from the Commonwealth of Massachusetts. Active Electrical Journeyman’s (Class B) or Master Electrician (Class A) license from the Commonwealth of Massachusetts.
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You will help to ensure the Trial Master File is up-to-date and inspection ready. As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards.
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Aiding in troubleshooting and resolving Master Data Management (MDM) issues, offering solutions aligned with master data strategies and best practices. Experience implementing large-scale, complex Master Data Management products.
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Ensure that CDM documentation is filed into the Trial Master File (TMF) according to SOPs and the study plans; review CDM files for completeness and accuracy. Ensure that CDM documentation is filed into the Trial Master File (TMF) according to SOPs and the study plans; review CDM files for completeness and accuracy.
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Organize, manage, and oversee the Trial Master File to maintain up-to-date regulatory documentation for all research sites. Be responsible for study laboratory sample management, including tracking and vendor management support.
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What You'll Need: 2+ years of professional experience in engineering mechanics, structural dynamics, and finite element analysis (FEA) with Master of Science or Master of Engineering in Structural Engineering - OR - 0+ years of professional experience in engineering mechanics, structural dynamics, and finite element analysis (FEA) with Doctorate in Structural Engineering Ability to obtain Professional Engineer (PE) or Structural Engineer (SE) registration within five years.
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As a Software Engineer on the OMS, you will work on a team consisting of a Product Manager, QA, Scrum Master, and other Software Engineers. Ask us about our values: True North, Master Your Craft, Clients are Our Context, Change is Opportunity, 1+1=3, and Deliver Excellence.
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AWS and Snowflake or other cloud-based data solutions and Master Data Management (MDM) experience. I am partnered with a large pharmaceutical company looking for an experienced commercial data management professional to serve as the Data Steward and to develop and lead data strategy and governance processes.
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Master Social Worker MSW - PRN. Speech Language Pathologist SLP - PRN. Master Social Worker MSW - PRN. LPNs: $35/hr - $40 / hour or $45 per visit. Occupational Therapist OT. Thursday, May 2nd from 9AM - 5PM CST.
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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
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Promote an overall positive experience for junior staff Serve as a role model by actively demonstrating and living BCG’s Culture and Values You Bring: Bachelors or Master degree in information technology, computer science, economics, supply chain, logistics or system engineering, business management/administration, or relevant field 5-8 years of practical experience in IT/ERP consulting, professional software development, product and program implementation.
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master job in Lexington, MA
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