Principal Scientific Writer at Novartis

, , Ireland -

Full Time

Start Date

Immediate

Expiry Date

08 Mar, 26

Salary

0.0

Posted On

08 Dec, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Scientific Writing, Clinical Research, Project Management, Content Creation, Process Improvement, Customer Management, Publication Planning, Training, Documentation, Compliance, Communication, Team Collaboration, Archiving, SOP Compliance, Scientific Communication, Meeting Materials Preparation

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary In this role you will be responsible for the creation of high-quality highly-complex 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. Job Description Major Activities Prepare / support the preparation of highly complex scientific documents to meet highest quality standards, including pivotal primary manuscripts, scientific communications platform and scientific lexicons, scientific writing for IEPs, meeting materials for satellite symposia, publication planning materials. Initiates/ implement and champion process improvement techniques. Manage multiple projects across multiple brands and therapeutic areas. Define and implement customer management strategies and tactics. Ideate and implement tactics to influence internal and external development environment. Comply with and support group’s project management tool, standards, policies and initiatives. Follow Novartis specifications for documentation, templates etc. Maintain records for all assigned projects including archiving. Maintain audit, SOP and training compliance. Train new joiners, fellow colleagues as and when required. Perform additional tasks as assigned. Education Minimum: Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience, M.Sc./M.Pharm +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 exp Languages: Excellent written and oral English Skills Desired Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

The Principal Scientific Writer is responsible for creating high-quality, complex scientific content and managing projects from brief to publication. This includes preparing pivotal manuscripts, scientific communications, and maintaining compliance with documentation standards.