"Scientific Writer I" @ Novartis Health Care Pvt. Ltd.

Novartis Healthcare Private Limited

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. 

Position Title: Scientific Writer I

Job Description:

• Prepares manuscripts, abstracts, posters, slide sets, 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.
• Performs quality control (QC) checking / proof reading of, abstracts, posters, slide sets and other scientific resources to meet customer expectations.
• Manages multiple projects at any given time.
• Comply with and support oncology scientific writing (OSW) group’s project management tool, standards, policies and initiatives.
• Follow Novartis specifications for documentation, specifically Novstyle, templates etc.
• Follow and track clinical trial milestones for assigned projects.
• Maintain records for all assigned projects including Datavision and other databases
• Maintain audit, SOP and training compliance.
• Contribute to development of processes within OSW group
• Support development of OSW group through participating in OSW group initiatives and other related activities.
• Builds working relationships and actively collaborates with key internal and external stakeholders to optimize feed-back and input towards high quality documents.
• Performs additional tasks as assigned.
• Participate in international congresses and conferences; development of pre and post congress scientific communication deliverables
Qualification:
• University life science degree or equivalent is required.
• Advanced degree or equivalent education/degree in life sciences/healthcare is desirable
• Masters with 3-5 years of experience.
• PhD or degree in medicine (MBBS/ MD or equivalent) with 1-3 years of experience. 
• Excellent written and oral English
Desirable:
•  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. 
How to Apply: Click to "Apply to Job" button given below.

Original Notification

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