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Senior Associate – Scientific Writing

0 years
Not Disclosed
10 Nov. 18, 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

Senior Associate – Scientific Writing

Location: Karnataka, India
Date Posted: 17 November 2025
Experience Required: Fresher eligible (0 years). Candidates with academic writing exposure, research internships, or scientific publishing experience will be considered.


About the Organization

We are a global, technology-driven healthcare solutions provider committed to helping healthcare organizations become future-ready. Our teams work at the intersection of science, digital technology, and healthcare transformation. Freshers entering this role will benefit from structured training, strong mentorship, and accelerated learning opportunities while contributing to high-impact scientific communication projects.


Role Overview: Senior Associate – Scientific Writing

This role supports the development of high-quality scientific and medical content for global healthcare and pharmaceutical clients. You will contribute to literature reviews, publication materials, scientific communication assets, and data-driven content. Freshers with a strong science background and passion for writing are encouraged to apply.


Key Responsibilities

Scientific Content Development

• Prepare and review scientific literature, abstracts, posters, manuscripts, slide decks, and publication materials
• Develop medically accurate, evidence-based scientific content aligned with branding and regulatory requirements
• Interpret and translate clinical study data from protocols, study reports, and peer-reviewed publications
• Ensure all outputs follow established scientific, editorial, and stylistic guidelines

Project Coordination and Quality Review

• Understand client requirements, scope, and service-level expectations at project initiation
• Conduct fact-checking, referencing, and verification using current scientific sources
• Respond to ad-hoc client requests within defined timelines
• Coordinate with medical writing leads, project managers, and design teams
• Review content prepared by junior contributors to ensure accuracy and compliance

Tools and Workflow Management

• Work with proprietary tools such as DataVision and PubsHub for publication tracking and version control
• Create project records, upload documents, update timelines, and manage publication attributes within the assigned tools
• Manage concurrent and sequential publication workflows


Desired Skills and Competencies

• Strong scientific writing skills and the ability to simplify complex data
• Excellent written and verbal communication skills
• Understanding of medical or therapeutic areas is an advantage
• Ability to stay updated with recent scientific advancements
• Strong proficiency in Microsoft Office tools
• Ability to collaborate effectively with cross-functional teams
• Initiative-driven, detail-oriented, and able to meet deadlines


Educational Qualification

• MPharm, PharmD, PhD, or a graduate in Life Sciences
• Freshers with academic scientific writing, thesis experience, research projects, or publication coordination exposure will be considered


Who Should Apply?

This role is ideal for fresh graduates seeking to start a career in:
• Scientific Writing
• Medical Affairs Content Development
• Publication Support
• Medical Communications
• Evidence-Based Medical Content Creation