Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Manager- Scientific Writing

Indegene
Indegene
8-12 years
preferred by company
10 Jan. 12, 2026
Job Description
Job Type: Full Time Hybrid 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

Associate Manager – Scientific Writing

Location: Karnataka, India
Employment Type: Full-Time | Hybrid/Office-Based
Job ID: [To be assigned]
Posted Date: 19 Dec 2025


About Indegene

Indegene is a technology-driven healthcare solutions provider committed to enabling healthcare organizations to be future-ready. By combining innovation, collaboration, and data-driven solutions, we deliver measurable impact to clients globally. At Indegene, you will experience accelerated career growth, mentorship from industry leaders, and the opportunity to work at the intersection of healthcare and technology. Explore more at Indegene Careers.


Role Overview

We are seeking a highly skilled Associate Manager – Scientific Writing to join our publication and medical communications team. This role requires expertise in scientific content development, publication management, and cross-functional coordination. The incumbent will ensure high-quality, scientifically accurate, and compliant deliverables across multiple therapeutic areas.


Key Responsibilities

  • Lead end-to-end publication management, including planning, timelines, and execution of scientific documents.

  • Develop and review abstracts, posters, oral presentations, manuscripts, slide decks, infographics, and other medical communications content.

  • Ensure all materials are scientifically accurate, medically relevant, and aligned with client branding and regulatory guidelines.

  • Understand and define client requirements at project kickoff, including SLAs, turnaround times, and project deliverables.

  • Conduct peer reviews and mentor junior writers for quality content output.

  • Maintain version control and publication timelines using proprietary tools such as DataVision and PubsHub PM Solution, managing concurrent, sequential, and hybrid workflows.

  • Respond to ad-hoc client requests within established deadlines.

  • Collaborate with medical writing leads, project managers, graphic teams, and clients to ensure seamless execution.

  • Ensure compliance with pharmaceutical regulations, publication guidelines, and ethical standards, using authentic and up-to-date references.


Required Skills & Qualifications

  • Experience: 8–12 years in medical writing, publication management, or pharmaceutical medical communications.

  • Strong proficiency in developing scientific content across multiple therapeutic areas.

  • Ability to coordinate end-to-end publication projects, including planning, execution, and tracking deliverables.

  • Excellent written and verbal communication skills; capable of direct client/author interaction.

  • Proficient in Microsoft Office tools and digital publication management solutions.

  • Educational Qualification: M.Pharm, PharmD, Ph.D., or life sciences graduate with relevant publication/medical writing experience.

  • Familiarity with clinical trial protocols, clinical study reports (CSRs), and scientific literature.


Preferred / Desirable Skills

  • CMPP certification (preferred).

  • Specialized knowledge in a therapeutic or medical specialty.

  • Strong analytical and research skills with attention to scientific accuracy.

  • Ability to stay updated with technical and scientific developments relevant to ongoing projects.

  • Strong organizational, multitasking, and time management abilities.


Why Join Indegene

  • Work with a global, technology-led healthcare organization driving innovation and transformation.

  • Accelerated career growth and exposure to high-impact projects across multiple therapeutic areas.

  • Mentorship and learning opportunities from industry experts.

  • Inclusive and collaborative work culture fostering diversity, equity, and inclusion.


Equal Opportunity Statement

Indegene is an Equal Opportunity Employer committed to fostering an inclusive and diverse workplace. Employment decisions are based on merit, qualification, and business requirements without discrimination based on race, religion, gender, sexual orientation, disability, veteran status, or any other legally protected characteristics.


SEO / Keyword Optimization:
Medical Writer Jobs India, Scientific Writer Jobs, Pharma Publication Manager, Medical Writing Careers, Medical Communications Jobs, Indegene Careers, Clinical Research Writing, Manuscript Development, Pharma Publications