Opportunity to work as Senior Scientific Writer at Novartis – Apply before 30th Oct’ 2024

Job Title: Senior Scientific Writer II
Company: Novartis

About Novartis

Novartis is a global healthcare company based in Switzerland. It is one of the world’s largest pharmaceutical companies, focusing on the research, development, manufacturing, and marketing of healthcare products. The company’s mission is to discover new ways to improve and extend people’s lives.

Novartis operates in various segments, including pharmaceuticals, eye care, and generic medicines. It is known for producing innovative medicines in areas such as oncology, immunology, dermatology, cardiovascular, renal, and metabolic conditions. Novartis has a strong commitment to research and development, investing heavily in cutting-edge technologies and new therapeutic solutions.

In addition to its pharmaceutical products, Novartis is also involved in initiatives to improve global health, including programs to combat neglected diseases and efforts to expand access to healthcare in underserved regions.

Join Novartis, where your work will contribute to bringing innovative medicines to life. As a Senior Scientific Writer II, you will be responsible for creating high-quality medical and scientific communications, including literature reviews, abstracts, posters, slide sets, and manuscripts. Your work will support internal medical, clinical, and regulatory teams and contribute to presentations at congresses and publications.

Key Responsibilities

• Prepare and deliver scientific documents such as literature reviews, abstracts, posters, slide sets, and manuscripts, using clinical study reports, protocols, and other data sources.
• Perform quality control (QC) checks and proofreading of deliverables to ensure accuracy and compliance with customer expectations.
• Manage multiple projects simultaneously, working on up to two brands at any given time.
• Collect and implement customer feedback to improve communications and content delivery.
• Follow Novartis documentation standards, such as Novstyle, templates, and guidelines for clinical trial milestones.
• Maintain project records, ensuring audit readiness and compliance with SOPs and training.
• Train and mentor new team members and colleagues as needed.
• Complete additional tasks as assigned to support the overall success of the team.

Candidate Profile

• Experience in preparing scientific documents to meet submission standards for regulatory authorities, clinical teams, and journals.
• Strong ability to adhere to publication standards, including CONSORT guidelines, and compliance with journal formatting requirements.
• Proficiency in English is essential.
• Educational qualifications include:
  • B.Sc./equivalent with 8+ years of Clinical Research (CR) experience
  • M.Sc./M.Pharma with 6+ years of CR experience
  • PhD with 4+ years of CR experience
  • MBBS or equivalent with 4+ years of CR experience
  • MD with 2+ years of CR experience

Additional Information

• Location: Hyderabad
• Business Unit: CTS
• Functional Area: Research & Development
• Application Deadline: 30th October 2024

At Novartis, you will work with diverse, talented, and driven individuals in one of the most rewarding and innovative industries. Apply today to be part of a team that is shaping the future of healthcare.

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