Associate Director Rwe Real World Evidence Manager Job In The Medicines Company In India, Uk

List of all associate director rwe real world evidence manager job in the medicines company in india, uk. Click Here View Job List. This page will help you to get all details about associate director rwe real world evidence manager job in the medicines company in india, uk. Associate Director Rwe Real World Evidence Manager job 2024 in the medicines company company in India, Uk location. Apply online for associate director rwe real world evidence manager vacancy in the medicines company.
Job Details
Job DescriptionJob Description CONEXTS is the unique trusted network of specialists partnering across all of Novartis delivering high quality services and innovative solutions to enable our enterprise goal of reimagining medicine The Associate Director will support RWE Executive Directors (or similar) as part of CONEXTS, in developing and executing RWE strategies for molecules within a disease area as well as the execution of Real World Evidence activities, in particular, non-interventional studies (NIS) The Associate Director Real World Evidence will support a franchise and lead key RWE projects and at the same time, provide strong technical contribution to enhance quality of deliverablesMajor Accountabilities1 Support the development and implementation of RWE strategies across multiple molecules with a service mindset, in collaboration with internal partners, to ensure that the value of our medicines is supported by evidence both globally and locally.

2 Support cross-functional Real World Evidence teams consisting of internal partners with the clear objective to deliver scientifically valid and robust evidence to support all stages of product development, and to drive global and local value demonstration3 Lead non-interventional studies and other RWD projects and stay current with and adopt emergent analytical methodologies, tools and applications to ensure fit-for-purpose and innovative approaches identify new ideas for RWE that are specific and measurable and promote an innovative mindset throughout the organization 4.

Apply rigor in study design and analytical methods design a fit-for-purpose analysis plan, assess innovative and more effective ways of presenting and delivering the results to maximize impact and interpretability implement and/or oversee the study, including its reporting ensure compliance with applicable pharma industry regulations and standards5 Drive RWE innovations and effective communication to internal stakeholders, regulatory, health technology assessment (HTA) bodies and scientific communities continuously strive to publish results in peer-review journals and conferences participate in external meetings and forums as a thought-leader (eg, congress/conference).

6 Lead functional, cross-functional, enterprise-wide or external RWE communities, networks, collaborations, initiatives or goals on knowledge-sharing, methodologies, innovations, technology, IT infrastructure, policy-shaping, processes, etc to enable broader and more effective use of data and analytics to reimagine cancer treatment 7 Lead effective communication on RWE activities and studies.

8 Support the development of the CONEXTS RWE service and contribute to the development of department-level standards, tools and templates and preparing 'best practices' and sharing in alignment with RWE Executive Director9 Mentor/coach colleagues to improve in their role with both personal and technical skills and help on-board new team members, as appropriate, and complete special projects as assignedDiversity & Inclusion / EEO Minimum Requirements Key RequirementsEducation: Master's degree in a field such as epidemiology, public health, biostatistics, statistics, bioinformatics, economics or similar.

Extensive relevant experience expected 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, public health, biostatistics, statistics, bioinformatics, economics or similar Relevant experience expected 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 industryExperience: Deep understanding and experience of Real World Data/Real World Evidence or related disciplines (e.

g, HEOR, outcomes research) to generate scientifically rigorous and value evidence from secondary data sources Experience/knowledge in causal inference methods including propensity score matching, inverse probability of treatment weights.

Strong experience and excellent knowledge of observational and/or epidemiological research and statistical methods Demonstrated track record of leading and executing research projects with no or minimal supervision using real world data from claims, electronic health records, registries, biobanks, and/or digital applications Proven ability to interpret, discuss and represent data relating to the assigned area.

Strong team spirit and service mindset Demonstrated ability to publish study results in peer-review journals and conferences.

Demonstrated experience with managing project scope and driving delivery in an evolving environment requiring proactivity and effective problem-solving and prioritization when faced with challenges Excellent collaboration and communication skills Proven ability to translate and communicate complex ideas, concepts and RWE solutions to diverse audiences.

Proven ability to work both independently and in a cross-functional team setting Proven ability to develop and successfully implement new strategies and ideas Well organized and results focused, ability to meet difficult timelines in a dynamic environment .

Action oriented - Excellent organization, interpersonal and influencing skills, ensuring delivery to target and expectations 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 opportunities.

Why 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!Join 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-N
Candidate Profile
The Medicines Company is looking for .

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

Short Job Information


Job Title : Associate Director Rwe Real World Evidence Manager
Company Name : The Medicines Company
Job Location : India, Uk
Education : Any Graduate / Post Graduate
Category : Medical
Experience : Freshers
Post Date : 15 March, 2023
Last Date : 03 June, 2023
Get Latest Job Alerts
We Need Your Resume
Post Resume Free
How to Apply for Associate Director Rwe Real World Evidence Manager
Other Similar Jobs to Associate Director Rwe Real World Evidence Manager
By Category
Post Your Resume Here