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Senior Scientific Writer I
Sandoz
posted 8hr ago
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Flexible timing
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Job Description
Job Description
Senior Scientific Writer I
Location - Hyderabad #LI Hybrid
About the Role:
Location - Hyderabad #LI Hybrid
About the Role:
To write, edit, reconcile and manage high quality medical and scientific communications including manuscripts, literature review, abstracts, posters, slide sets for publication/presentation or for submission to regulatory authorities and/or clinical teams.
Key Responsibilities:
Prepares manuscripts, literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles, protocols etc.
Performs quality control (QC) checking / proof reading of literature review, abstracts, posters, and slide sets to meet customer expectations. Manages up to two assigned team projects at any given time.
Ensures getting feedback from customers and supports implementation of customer management tactics.
Comply with and support 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 archiving.
Maintain audit, SOP and training compliance. 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.
Role Requirements :
Essential Requirements
Minimum science degree or equivalent, B.Sc./equivalent with 6 years Clinical Research (CR) experience, M.Sc./M.Pharma +4 years of clinical research (CR) experience.
Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent).
Desirable Requirements:
PhD + 2 year of CR experience, MBBS/equivalent + 2 year of CR experience, MD +1 year of CR experience
Excellent written and oral English.
Why Novartis: Our purpose is to reimagine medicine to improve and extend people s 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:
You ll 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-rewards
https: / / talentnetwork.novartis.com / network.
Minimum science degree or equivalent, B.Sc./equivalent with 6 years Clinical Research (CR) experience, M.Sc./M.Pharma +4 years of clinical research (CR) experience.
Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent).
Desirable Requirements:
PhD + 2 year of CR experience, MBBS/equivalent + 2 year of CR experience, MD +1 year of CR experience
Excellent written and oral English.
Why Novartis: Our purpose is to reimagine medicine to improve and extend people s 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:
You ll 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-rewards
https: / / talentnetwork.novartis.com / network.
Skills Desired
Clinical Research, Clinical Trials, Detail-Oriented, Medical Writing, Regulatory Compliance, Safety Employment Type: Full Time, Permanent
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Flexible timing
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