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Senior Scientific Writer

Senior Scientific Writer

NOVARTIS

8 - 13 years

25 - 30 Lacs

hyderabad

Posted:1 day ago| Platform:

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Skills Required

publishing compliance project management diversity and inclusion clinical research archiving representative manager quality control proof reading auditing

Work Mode

Work from Office

Job Type

Full Time

Job Description

Creation of high-quality scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery.

About the Role

Senior Scientific Writer

Location - Hyderabad #LI Hybrid

About the Role

Key Responsibilities

Prepares abstracts, posters, and presentation slide sets, manuscripts (subgroup analysis, RWE/observational studies), medical resources (literature searches, publication alerts, congress communications, study decks), medical education materials, congress support materials (pre-congress material, onsite-coverage, post-congress decks, content for omni channel).
Performs quality control (QC) checking / proof reading of the above-mentioned deliverables to meet customer expectations.
Manages multiple projects of up to two brands at any given time.
Obtains feedback from customers and implements customer management tactics.
Complies with and support group s project management tool, standards, policies and initiatives.
Follows Novartis specifications for documentation, templates etc.
Maintains records for all assigned projects including archiving.
Maintains audit, SOP and training compliance.

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Essential Requirements

Minimum science degree or equivalent, B.Sc./equivalent with 8 years Clinical Research (CR) experience, M.Sc./M.Pharm +6 years of clinical research (CR) experience
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 experience
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
Meeting set quality standards and on time for submission to Health Authorities/ Clinical teams / Journals as appropriate. (i.e. complying with standards e.g. CONSORT regarding publication of trial results, complying with journal formatting requirements etc).

Desirable Requirements

Excellence in communicating effectively across different audiences and organizational levels.
Excellence in designing and continuously improving business processes to meet quality and compliance standards and to simplify the way we work.
Proven ability to build strong and effective relationships with internal and external customers.

Benefits and Rewards

Read our handbook to learn about all the ways we ll help you thrive personally and professionally

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Senior Scientific Writer