Job Description

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 xe2x80x93 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 groupxe2x80x99s 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 peoplexe2x80x99s 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-cultureYouxe2x80x99ll 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

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