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DMCQ-0, Senior Specialist, Data Quality

4.00 to 9.00 Years   Bangalore   09 Sep, 2022
Merck Ltd
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

    A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.Your role: an exciting opportunity has arisen to join our healthcare business to support the development of first and best in class specialty medicines for our patients in need. As a Senior Data Quality Specialist, you will be working closely together with our Program and Trial Data Managers, and other data stewards to drive value creation by assessing the completeness, quality, and integrity of clinical and operational data by using advanced tools. You will leverage those tools for applicable studies to ensure key risk indicators (KRIs) for clinical data, and key quality indicators (KQIs) for operational data are properly defined. Furthermore, you will support the assessment of the Data Standards Quality of clinical study including datasets, documentation (cSDRG) and define.xml. Additionally, you will be accountable for establishing and maintaining effective program and study level communications with the respective Program, Trial Data Managers, and other key data stewards.Who you are:Advanced degree in Life Sciences (e.g. biology, chemistry, pharmaceuticals), Mathematics, Computer Sciences, or equivalent industry experienceProven experience (minimum 4-7 years) as a Clinical Data Manager or Data Analyst in the pharmaceutical/biotechnology industry or in the field of Centralized Clinical MonitoringStrong written and verbal communication skills in the English languageResults and detail-oriented approach to work, good understanding of programming language, data visualization, and proficient Computer Skills e.g. word processing, Excel, PPTExcellent Knowledge of Clinical Data Management Systems/EDC (e.g. Inform, Medidate Rave, Oracle RDC)Deep understanding of clinical operation is preferredComprehensive CDISC SDTM knowledge as well as deep knowledge of ICH-GCP and major health authority (e.g. FDA, EMA, NMPA, PMDA) regulationsAbility to work on multiple projects and manage competing prioritiesWhat we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!Curious Apply and find more information at https://jobs.vibrantm.com,

Keyskills :
active directorytroubleshootingenvironmentwindowsslaclinical data managementdata qualitydata analysislife sciencesclinical datadata standardsvalue creation

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