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Associate Manager- Scientific Writing

Indegene
Indegene
8-12 years
preferred by company
10 Jan. 20, 2026
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

Job Title: Associate Manager – Scientific Writing
Location: Karnataka, India
Job Type: Full-Time
Experience Required: 8–12 Years
Posted On: 17 January 2026


About the Company

Indegene is a technology-led healthcare solutions provider enabling healthcare organizations to become future-ready. Operating at the intersection of healthcare and technology, Indegene partners with global life sciences companies to deliver innovative, data-driven, and compliant scientific and medical communications. The organization fosters a purpose-driven culture rooted in innovation, collaboration, empathy, and customer obsession, while offering accelerated global career growth opportunities.


Job Overview

Indegene is seeking an experienced Associate Manager – Scientific Writing to lead and deliver high-quality scientific publications and medical communications. This role requires end-to-end expertise in publication planning, execution, and compliance, along with strong stakeholder management and mentoring capabilities. The position is ideal for professionals passionate about scientific writing, publications management, and global medical communications.


Key Responsibilities

  • Lead end-to-end publication management, including publication planning, execution, and delivery

  • Develop, review, and finalize complex scientific documents such as abstracts, manuscripts, posters, oral presentations, and slide decks using multiple data sources (clinical study reports, protocols, etc.)

  • Create and review medical communication materials including scientific communication platforms, plain language summaries (PLS), and infographics

  • Ensure all content is scientifically accurate, medically relevant, compliant with pharma regulations, publication guidelines, and branding standards

  • Define client requirements during project kick-off, including SLAs and turnaround timelines

  • Perform scientific fact-checking across therapeutic areas using authentic and up-to-date references

  • Handle ad-hoc client requests within defined timelines

  • Coordinate closely with medical writing leads, project managers, graphics teams, and clients

  • Conduct peer reviews and mentor junior writers to meet client and quality expectations

  • Manage publication workflows using proprietary tools such as DataVision and PubsHub PM Solution, including version control, timeline management, milestones, citations, and workflow tracking

  • Maintain effective written and verbal communication with clients, authors, and internal stakeholders


Required Skills & Experience

  • 8–12 years of hands-on experience in publication writing within pharmaceutical companies or medical communications agencies

  • Proven expertise in scientific publications and medical writing

  • Strong understanding of pharmaceutical regulations, ethical guidelines, and publication standards

  • Experience working with publication management tools such as DataVision and PubsHub (preferred)

  • Excellent written, verbal, and client-facing communication skills

  • Ability to manage multiple projects, concurrent workflows, and tight deadlines


Preferred Qualifications

  • CMPP certification (preferred)

  • M.Pharm, PharmD, PhD, or any Life Sciences graduate with strong publication or medical writing experience

  • Understanding of a specific therapeutic area or broad medical knowledge

  • Proficiency in Microsoft Office tools

  • Passion for scientific writing, continuous learning, and staying updated with emerging scientific developments


Equal Opportunity Statement

Indegene is an Equal Opportunity Employer committed to fostering an inclusive and diverse workplace. Employment decisions are based solely on business requirements, merit, and qualifications, without discrimination on the basis of race, religion, gender, age, disability, sexual orientation, or any other protected characteristic.


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