- Bangalore, is a department within the Clinical Drug Development area.
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Medical Reviewer
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Medical Reviewer
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Medical Reviewer
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Medical Reviewer
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Quality Medical Reviewer
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Associate Medical Reviewer
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Associate Medical Reviewer
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Associate Medical Reviewer
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Medical Reviewer Ags
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Alcon Bengaluru, IndiaSummary of Position: · - Alcon is looking to hire Medical Reviewer who performs_ · - Medical Safety activities for assigned Alcon projects or products, supporting the identification and comprehensive assessment of safety signals from all sources (clinical development through post ...
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Associate Medical Reviewer
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41268-assoc Medical Data Review Mg
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IQVIA Bengaluru, IndiaJob Overview · Provide comprehensive Medical Review expertise to provide efficient, quality data management products that meet customer needs. Provide project management support in the areas of structured patient data review per clinician's perspective. · Essential Functions · - ...
Associate Medical Reviewer - Bengaluru, India - Novo Nordisk
Description
Key Responsibilitiesin this position will be to perform Medical Review of all trial subjects of all assigned clinical trials within drug development portfolio across therapy areas & to ensure high quality consistent medical data.
Medical Review is performed for all trial subjects to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and Standard Operating Procedure (SOPs).
Associate Medical Reviewer ensures high quality medical data through medical review of clinical trial data.Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s) and Medical Specialists during trial conduct.
Report status of medical review to project as appropriate, following the project communication plan and blinding plan.Consult with Trial Managers and Medical Specialists as appropriate to ensure medical review issues are escalated in a timely manner.
Responsible for contribution to or participation in trial planning activities related to medical review.Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites.
Responsible for presenting findings of Medical Review to relevant Medical Specialist to enable decision making. Responsible for documenting medical review in the sponsor TMF.Ensure close collaboration with relevant study group members, especially the Data Manager , Trial Manager(s) and Medical Specialist during trial conduct.
Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform Medical review.
The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review.
Qualifications Minimum as Graduate in Medicine or other relevant (MBBS & MD in pharmacology preferred, MBBS & MD in other clinical/paraclinical areas with relevant experience in clinical patient management/ clinical research).
1-2 years of experience as a Medical Reviewer is preferred.Good knowledge of ICH (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use), GCP (Good clinical Practice).
Demonstrated computer skills (MS Office, MS Project, PowerPoint). Excellent understanding of medical terminology and clinical trial activities. Excellent written and spoken English. About the department The Centralised Monitoring Unit (CMU)Associate Medical reviewers actively involved in Risk-based medical monitoring in collaboration with the medical specialists from Denmark, with a focus on ensuring overall patient safety and wellbeing of all clinical trial participants, by ensuring compliance to protocol and identifying potential clinically significant outliers that require medical attention and medical data cleaning.
The Functional Programmers develop operational visualizations in data visualization tools to support the trial teams on proactive centralized monitoring and Statistical Monitors perform detection of unusual data patterns, systematic errors and potential lack of compliance or fraud across trials.
Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a -year legacy of driving change to defeat serious chronic diseases.
Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily.
All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63, employees around the world.We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them.
Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us Together, we go further. Together, we're life-changing.