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Senior Scientific Writer Ii

6+ years
Not Disclosed
10 Jan. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Senior Scientific Writer II
Location: Hyderabad, India (Hybrid)

About the Role:
The Senior Scientific Writer II is responsible for writing, supporting, and managing projects to prepare high-quality medical and scientific communications. This includes literature reviews, abstracts, posters, slide sets, and sophisticated manuscripts for publication or presentation at congresses or internal medical and clinical teams.

Key Responsibilities:

  • Prepare literature reviews, abstracts, posters, slide sets, and sophisticated manuscripts based on clinical study reports, patient profiles, protocols, and other data sources.
  • Perform quality control (QC) checking and proofreading of all deliverables to ensure they meet customer expectations.
  • Handle multiple projects (up to two brands) at any given time, acquiring customer feedback and implementing customer management tactics.
  • Support the use of project management tools, standards, policies, and initiatives within the group.
  • Ensure compliance with Novartis documentation specifications, including following templates and Novstyle.
  • Track clinical trial milestones and maintain records for assigned projects, including archiving.
  • Ensure adherence to audit, SOP, and training requirements.
  • Train new joiners and colleagues, as required, and perform additional tasks as assigned.

Commitment to Diversity & Inclusion:
Novartis is committed to building an inclusive work environment and diverse teams that reflect the patients and communities we serve.

Role Requirements:
Essential Requirements:

  • B.Sc./M.Sc./M.Pharma/MBBS/PhD/MD with proficiency in English and a minimum of 6–8 years of Clinical Research (CR) experience.
  • Experience in the preparation of high-quality scientific documents (literature reviews, abstracts, posters, manuscripts) according to standards such as CONSORT for clinical trial results.
  • Proven ability to manage projects and handle multiple tasks within set timelines.

Desirable Requirements:

  • Doctoral degree or qualification in Medical Sciences (MBBS/MD/equivalent).
  • PhD + 4 years of CR experience, or MD + 2 years of CR experience.

Why Novartis:
Our purpose is to reimagine medicine to improve and extend people’s lives. Our vision is to become the most valued and trusted medicines company in the world, and we achieve this through the talent and dedication of our people. Learn more about us at Novartis Strategy.

You’ll Receive:
Explore everything you need to know about our benefits and rewards in the Novartis Life Handbook.

Join Our Novartis Network:
If this role isn’t the right fit for you, stay connected and hear about future opportunities by joining the Novartis Network: Novartis Talent Network.

Benefits and Rewards:
Find out how we support our associates' personal and professional growth in the Benefits Handbook.

Division: Operations
Business Unit: Innovative Medicines
Location: Hyderabad, India
Company/Legal Entity: Novartis Healthcare Private Limited
Functional Area: Research & Development
Job Type: Full-time, Regular
Shift Work: No