Rwe Specialist Job In The Medicines Company In India, Ireland

Job DescriptionJob Description The Real World Evidence (RWE) Specialist will work with the Global RWE teams (including RWE Directors in Global Patient Access and RWE Scientists in Global Medical Affairs) and Novartis country organizations to support the execution of Real World Data (RWD) projects and, in particular, non-interventional studies (NIS) The RWE Specialist will support a franchise, and will help enable RWE study execution, documentation, communication, and sharingMajor Accountabilities1 Support project management of non-interventional studies and other RWD projectso Prepare of project plans, eg.

including governance processes, milestone tableso Organize key project meetings, eg including slides for project updates and discussionso Support project tracking and reporting, eg to regional, country, Global and COE stakeholderso Support operational aspects of vendor management e.

g incl contracting activities to license and onboard database(s) , as necessaryo Manage internal project management, study governance and review systems2 Support effective communication on RWE activities and studieso Facilitate effective communication of research findings internally and externally through development of slide decks, yammer posts and other communication toolso Support development of an efficient and targeted RWE publications plano Support review of abstracts, posters and manuscriptso Ensure that timelines of the publications development are met3.

Support implementation of non-interventional studieso Support NIS document (concept sheet, protocol, analysis plan, report) preparation, eg review of literature for related studies, best practices, etco Work with other Real World Evidence teams and medical experts to generate and align on code lists to be used for RWE study variable generation and other study inputs 4 RW data related activitieso Support franchise, and CPOs with identifying RWD sources (e.

g data mapping via literature reviews and desk research)o Support franchises and CPOs with licensing, governance, and onboarding of new RWD sources 5 Contribute to department initiatives and to the development of department-level standards, tools and templates and preparing 'best practices' and sharing in alignment with RWE Director/Scientist 6 Help on-board new team members, as appropriate, and complete special projects as assignedDiversity & Inclusion / EEO Minimum Requirements Key RequirementsEducation:Bachelor's/Master's degree in a field such as epidemiology, biostatistics, statistics, bioinformatics, economics or similar And some relevant experience conducting research in the pharma industry, contract research organization, healthcare provider / HTA or academic institute or experience in a closely related discipline within the pharma industry.

OrPhD in a field such as epidemiology, biostatistics, statistics, bioinformatics, economics or similar Experience in project management within a global/matrix environment in the pharmaceutical industry or relevant consultancy Strong interpersonal skills-ability to quickly build relationships.

Prior work experience of RWE execution in a pharmaceutical company or contract research organization is considered a plus Prior work experience with data from electronic medical records, registry databases and external insurance claims databases is considered a plus Proven ability to interpret, discuss and represent data relating to the assigned area .

Proven ability to work both independently and in a cross functional team setting Action oriented - Excellent organization skills, ensuring delivery to target and expectations Informing - Provides relevant and timely updates to stakeholders, ensuring issues are raised early.

Managing and measuring work - Ensures plans are kept up to date and status is regularly reported Perseverance - Skills in driving outcomes to meet customer needs, with an understanding of how to overcome challenges to meet tight schedules Strong written/verbal communication skills.

Highly effective at providing input at meetings, discussions and activities covering aspects of research data management and analysis on research projectsYou'll receive:Competitive salary, Annual bonus, Pension scheme, Share scheme, Health insurance, 25 days annual leave, Flexible working arrangements, subsidised dining facilities, Employee recognition scheme, learning and development opportunitiesWhy consider Novartis769 million lives were touched by Novartis medicines in 2020, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges Because the greatest risk in life, is the risk of never trying! Imagine what you could do at Novartis!Novartis Ireland Ltd has been certified as a Top Employer 2021 by the Top Employers Institute for its exceptional employee offeringsJoin our Novartis Network:If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: #LI-NOV = Novartis

The Medicines Company is looking for .

The Medicines Company is looking for Any Graduate / Post Graduate profile candidates.