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Novartis Healthcare Pvt Ltd

Novartis (NYSE: NVS) is a world leader in the research and development of products to protect and improve health and well-being. The company has core businesses in pharmaceuticals, vaccines, consumer health, generics, eye care and animal health. Headquartered in Basel, Switzerland, Novartis employs nearly 115 000 people in over 140 countries worldwide to help save lives and improve the quality of life. The Group is present in India through Novartis India Limited, listed on the Mumbai Stoc... Read More

Address      Sandoz House Shivsagar Estate Dr Annie Besant Road Worli, Mumbai India
Website      www.novartis.in/
Holding      No Holding Details

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Senior Scientific Writer II

To write, support and manage projects to prepare high quality scientific communications including, abstracts, posters, slide sets, manuscripts (complex) for publication/ presentation, monographs, flash cards pub alerts, literature reviews and other scientific resources 1.Prepares complex manuscripts, abstracts, posters, slide sets, and monographs, flash cards, pub alerts literature reviews and other scientific resources working from various data sources including data tables and graphics, FIR reports, clinical study reports, patient profiles, protocols etc. 2.Performs quality control (QC) checking / proof reading of the above mentioned deliverables to meet customer expectations. 3.Manages multiple projects of up to two brands at any given time. 4.Complies with and support oncology scientific writing (OSW) groups project management tool, standards, policies and initiatives. 5.Follows Novartis specifications for documentation, specifically Novstyle, templates etc. 6.Follows and tracks clinical trial milestones for assigned projects. 7.Maintains records for all assigned projects including Datavision and other databases 8.Maintains audit, SOP and training compliance. 9.Contribute to development of processes within OSW group 10.Support development of OSW group through participating in OSW group initiatives and other related activities. 11.Builds working relationships and actively collaborates with key internal and external stakeholders to optimize feed-back and input towards high quality documents. 12.Trains new joiners, fellow colleagues as and when required. 13.Performs additional tasks as assigned. 14.Participate in international congresses and conferences; development of pre and post congress scientific communication deliverables Desired Profile Minimum: University life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable: Masters with 4-6 years of experience. PhD or degree in medicine (MBBS/ MD or equivalent) with 2-4 years of experience. Excellent written and oral English Scientific/ Clinical Knowledge of Safety aspects, TA, Disease, Brand Experience and/or knowledge of Oncology preferred. Experience of writing publications, abstracts, slidesets, posters, manuscripts and/or other educational re-sources Good understanding clinical research and drug development process Experience of working in cross-functional teams in the drug development industry. Experience 4 - 6 Years Industry Type Pharma / Biotech / Clinical Research Role Documentation/Medical Writing

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