Senior Scientific Writer II

NOVARTIS

8 - 13 years

25 - 30 Lacs

hyderabad

Posted:3 days ago| Platform:

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Skills Required

customer management literature networking project management diversity and inclusion clinical research archiving manager quality control proof reading auditing

Work Mode

Work from Office

Job Type

Full Time

Job Description

To write, support and manage projects, to prepare high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, manuscripts (complex) for publication/ presentation at congresses or internal medical and/or clinical teams.

About the Role

Senior Scientific Writer II

Location - Hyderabad #LI Hybrid

Major Responsibilities

Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) 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.
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, specifically Novstyle, templates etc. Follows and tracks clinical trial milestones for assigned projects.
Maintains records for all assigned projects including archiving.
Maintains audit, SOP and training compliance. Train new joiners, fellow colleagues as and when required. Performs additional tasks as assigned.

Minimum Requirements

Minimum Education - 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.
Desired - 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.

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