Instagram
youtube
Facebook

Lead Expert - Scientific Writer

8+ years
Not Disclosed
10 Dec. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Lead Expert – Scientific Writer

Job ID: 294244
Location: Bengaluru, Karnataka, India
Job Type: Full-Time


About the Organisation

The company is a global leader in Healthcare, Life Sciences, and Technology, committed to advancing science and improving lives. With teams across six continents, the organisation combines innovation, research excellence, and a strong patient-centric mission. Its healthcare division focuses on developing advanced medicines, intelligent devices, and breakthrough technologies in key therapeutic areas such as Oncology, Neurology, Immunology, Fertility, and Cardio-Metabolic Disorders.

The Global Scientific Communications Content Hub in Bengaluru is a high-performing, collaborative division responsible for medical communication, medical information, and medical education content for global medical units. The organisation is now expanding its scientific writing capability and seeking senior-level scientific writing professionals to strengthen its global operations.


Position Overview

The Lead Expert – Scientific Writer will be responsible for developing, reviewing, and leading the creation of high-quality medical and scientific content across therapeutic areas. This role involves overseeing medium- to high-complexity projects, guiding junior writers, ensuring scientific accuracy, and maintaining alignment with strategic communication objectives.

The ideal candidate will have advanced scientific writing experience, strong project leadership capability, and the ability to collaborate effectively with global stakeholders.


Key Responsibilities

  • Develop high-quality scientific and medical content for multiple project types, including publications, congress materials, medical communication documents, and medical education materials.

  • Independently lead medium- to high-complexity content development and guide other writers through review and quality assessment.

  • Review scientific outputs produced by junior writers to ensure accuracy, tone consistency, and alignment with strategic messaging.

  • Lead content development meetings with authors, experts, and cross-functional stakeholders.

  • Act as subject matter expert for assigned therapy areas and assets.

  • Mentor junior writers and implement programs to strengthen team capabilities.

  • Maintain strong working relationships with global medical units and internal stakeholders.

  • Manage project timelines, prioritize tasks effectively, and ensure personal productivity targets are achieved.

  • Provide clear project status updates and ensure timely, high-quality delivery of assigned work.

  • Contribute to process improvement initiatives within the Global Scientific Communications Content Hub.


Experience Requirements

  • Minimum 9 years of professional experience in scientific writing, medical communications, medical affairs, or clinical research within a pharma, biotech, or medical communications agency environment.

  • Proven experience leading complex writing projects and delivering diverse content types simultaneously.

  • Strong background in therapeutic areas such as Oncology, Neurology, Immunology, Fertility, Cardio-Metabolic Disorders, or Endocrinology.

  • Demonstrated experience working in international and cross-functional settings.


Educational Requirements

  • Advanced degree in Science, Medicine, Pharmacy, or related disciplines.

  • Higher academic qualifications (PhD, MD, MPharm, MSc) are preferred for this role.


Key Skills and Competencies

  • Strong scientific writing expertise with the ability to simplify complex scientific concepts for diverse audiences.

  • Excellent understanding of pharmaceutical industry practices, medical affairs, and evolving industry trends.

  • Strong stakeholder management and interpersonal communication skills.

  • Ability to manage multiple projects simultaneously, prioritize effectively, and meet tight deadlines.

  • Strong analytical skills, with the ability to understand complex scientific data and project workflows.

  • Excellent verbal and written communication skills in English.


Work Environment and Culture

The organisation is committed to diversity, inclusion, equal opportunity, and building a workplace where every individual can grow and contribute. Employees are supported through flexible working practices, global collaboration opportunities, and continuous learning frameworks.


Equal Opportunity Statement

The company maintains a strict non-discrimination policy across all employment processes, including recruitment, promotions, compensation, and workplace conduct. Discrimination based on race, religion, age, sex, disability, sexual orientation, marital status, gender identity, national origin, or any protected classification is prohibited.


Fraudulent Job Offer Advisory

The organisation is aware of fraudulent recruitment communications circulating under its name. Applicants should verify the legitimacy of any job correspondence and avoid responding to messages that do not originate from official company communication channels.