05/09/2025 Senior Scientific Writer Ii

Summary Summary To write support and manage projects to prepare high quality medical and scientific communications including literature review abstracts posters slide sets Manuscripts sophisticated for publication presentation at congresses or internal medical and or clinical teams Senior Scientific Writer IILocation Hyderabad LI HybridAbout the Role To write support and manage projects to prepare high quality medical and scientific communications including literature review abstracts posters slide sets Manuscripts sophisticated for publication presentation at congresses or internal medical and or clinical teams Key Responsibilities Prepares literature review abstracts posters and slide sets and Manuscripts sophisticated working from various data sources including clinical study reports patient profiles protocols etc Performs quality control QC checking proof reading of the above mentioned deliverables to meet customer expectations Handles multiple projects of up to two brands at any given time Acquires feedback from customers and implements customer management tactics Complies with and support groups project management tool standards policies and initiatives Follows Novartis specifications for documentation specifically Novstyle templates etc Follows and supervises clinical trial milestones for assigned projects Maintains records for all assigned projects including archiving Maintains audit SOP and training compliance Trains new joiners fellow colleagues as and when required Performs additional tasks as assigned Commitment to Diversity Inclusion We are committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve Essential Requirements Preparation of the above referenced documents meeting set quality standards and on time for submission to Health Authorities Clinical teams Journals as appropriate i e staying in sync with standards e g CONSORT regarding publication of trial results complying with journal formatting requirements etc Timely preparation of medical and scientific documents to meet regulatory requirements for publication of clinical trial results to increase customer awareness of company products and to support marketing activities B Sc M Sc or M Pharma MBBS PhD MD Proficiency in English B Sc equivalent with 8 years Clinical Research CR experience M Sc M Pharma 6 years of clinical research CR experience Desirable Requirements Doctoral Degree or Qualification in Medical Sciences MBBS MD equivalent PhD 4 year of CR experience MBBS equivalent 4 year of CR experience MD 2 years of CR exp Why Novartis Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world How can we achieve this With our people It is our associates that drive us each day to reach our ambitions Be a part of this mission and join us Learn more here https www novartis com about strategy people-and-cultureYoull receive You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook https www novartis com careers benefits-rewardsJoin our Novartis Network If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities join the Novartis Network here https talentnetwork novartis com network Skills Desired Clinical Research Clinical Trials Detail-Oriented Medical Writing Regulatory Compliance Safety