Principal Scientific Writer

328201BR
Oct 12, 2021
India

Job Description

108,000 people reimagining medicine for more than 799 million people globally. Be part of this journey by representing a group that delivers medical communication solutions across multiple franchises, business units and affiliates. Our services and customized solutions enhance the reach of clinical data about relevant therapeutic advancements and supports in right treatment decisions. We support scientific writing, medical communications plan development, innovative ways of evidence dissemination, supporting our colleagues in medical affairs organization.

Your responsibilities include, but are not limited to:

• Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards. Initiates, implements and champions process improvement techniques.
• Manages multiple projects across multiple brands and therapeutic areas. Defines and implements customer management strategies and tactics.
• Develops a Center of Excellence (CoE) for identified TA/disease area/deliverable. Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion.
• Ideates and implements tactics to influence internal and external development environment. Supports people and performance management. Complies with and support group’s project management tool, standards, policies and initiatives.
• Follows Novartis specifications for documentation, specifically Novstyle, templates etc. Follows and track 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.

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

Minimum Requirements

• Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience,
• M.Sc./M.Pharma +10 years of clinical research (CR) experience. Desired – Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent) PhD > 8 year of CR experience, MBBS/equivalent >8 year of CR experience, MD >6 years of CR experience
• Excellent written and oral English. Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards
• Customer / partner/ project feedback and satisfaction. Adherence to Novartis policy and guidelines
• Collaborating across boundaries. Functional Breadth; Operations Management and Execution
• Project Management; Representing the organization.

WHY NOVARTIS
769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Join 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
CTS
NBS CONEXTS
India
Hyderabad, AP
Research & Development
Full Time
Regular
No
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328201BR

Principal Scientific Writer

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