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Senior Scientific Writer Ii

Novartis
Novartis
4-8 years
Not Disclosed
Hyderabad
1 May 6, 2026
Job Description
Job Type: Full Time Hybrid 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. Skills: Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern

Senior Scientific Writer II

Location: Hyderabad (Hybrid Office Model)
Job Type: Full-Time
Experience Required: 4–8+ Years in Clinical Research or Medical Writing
Application Deadline: May 7, 2026
Industry: Pharmaceutical / Clinical Research / Medical Communications


Job Overview

We are seeking an experienced and highly detail-oriented Senior Scientific Writer II to develop, manage, and deliver high-quality medical and scientific communication materials for publications, congress presentations, and internal medical or clinical teams. The selected candidate will be responsible for preparing scientifically accurate documents, managing multiple writing projects, supporting quality control activities, and collaborating with cross-functional stakeholders in a global pharmaceutical environment.

This role is ideal for professionals with strong expertise in medical writing, clinical research, scientific communication, and publication development.


Key Responsibilities

Scientific Writing & Medical Content Development

  • Prepare and develop:
    • Literature Reviews
    • Abstracts
    • Posters
    • Slide Decks
    • Scientific Manuscripts
    • Meeting Reports
    • Medical Communication Materials
  • Work with multiple data sources including:
    • Clinical Study Reports (CSR)
    • Patient Profiles
    • Clinical Protocols
    • Safety Data
    • Scientific Publications
  • Ensure all content is scientifically accurate, evidence-based, and aligned with publication standards.

Quality Control & Compliance

  • Perform:
    • Quality Control (QC) reviews
    • Proofreading
    • Data verification
    • Formatting validation
  • Ensure deliverables meet customer expectations and organizational quality standards.
  • Follow established:
    • SOPs
    • Documentation standards
    • Templates
    • Compliance procedures
  • Maintain audit readiness and proper project archiving/documentation.

Project & Stakeholder Management

  • Manage multiple projects across up to two brands simultaneously.
  • Coordinate with:
    • Internal medical teams
    • Clinical teams
    • Customers
    • Cross-functional stakeholders
  • Implement customer management strategies and incorporate stakeholder feedback effectively.
  • Support operational excellence and project management initiatives within the team.

Training & Team Support

  • Train and mentor:
    • New joiners
    • Team members
    • Junior colleagues
  • Contribute to:
    • Knowledge sharing
    • Process improvement
    • Team development initiatives
  • Perform additional responsibilities as assigned by leadership.

Required Qualifications

Educational Qualifications

Candidates must possess one of the following qualifications:

Bachelor’s / Master’s Degree Path

  • B.Sc. or equivalent degree with 8 years of Clinical Research experience
  • M.Sc. / M.Pharm with 6 years of Clinical Research experience

Medical / Doctoral Degree Path

  • MBBS or equivalent degree with 4 years of Clinical Research experience
  • PhD with 4 years of Clinical Research experience
  • MD with 2+ years of Clinical Research experience

Preferred Qualifications

  • Advanced qualifications in:
    • Medical Sciences
    • Clinical Research
    • Pharmacology
    • Healthcare Sciences
  • Certifications in:
    • Medical Writing
    • Clinical Research
    • Drug Development
    • Regulatory Writing
    • Project Management

Experience Requirements

  • Minimum 4–8+ years of experience in:
    • Clinical Research
    • Medical Writing
    • Scientific Writing
    • Pharmaceutical Communications
  • Experience in:
    • Drug Development
    • Clinical Trial Documentation
    • Medical Publications
    • Safety Documentation
  • Strong understanding of:
    • Scientific and clinical communication standards
    • Publication development workflows
    • Medical terminology and disease areas