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Thermo Fisher Careers 2026 | Associate Medical Writer Jobs Mumbai RemoteThermo Fisher Hiring | Associate Medical Writer Mumbai (Hybrid / Remote)Thermo Fisher Scientific (PPD) Bachelor's / Master's Degree in Scientific Discipline (B.Pharm/M.Pharm/PharmD/MSc) 1 to 3 Years Medical / Scientific Writing Experience Are you searching for associate medical writer jobs in Mumbai, PPD Thermo Fisher medical writing careers, or remote scientific writing vacancies for pharmacy and life science graduates Global leader in serving science Thermo Fisher Scientific (PPD Clinical Development) is hiring an Associate Medical Writer for its medical writing team in Mumbai, Maharashtra on a Hybrid / Remote basis. Job OverviewCompany: Thermo Fisher Scientific / PPD Clinical DevelopmentJob Title: Associate Medical WriterDepartment: Global Medical Writing & Clinical OperationsEmployment Type: Full-Time, PermanentRequired Experience: 1 to 3 Years in Scientific Writing or Pharma/CRO IndustryQualifications: B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc in Science or PharmacyCore Deliverables: Informed Consent Forms (ICFs), Lay Summaries, Quality Audits, MS TemplatesAs an Associate Medical Writer at Thermo Fisher, your core duties will include: Patient-Centric Document Writing: Research, draft, and edit routine patient-centric documents including Informed Consent Forms (ICFs), assent forms, and plain language Lay Summaries.Clinical & Program Documentation: Assist senior medical writers in drafting more complex clinical trial protocols, clinical study reports (CSRs), and investigator brochures.Quality & Compliance Review: Ensure all assigned documents comply with internal quality control checklists, client style guides, and ICH-GCP regulatory guidelines.Project Management Support: Assist with developing document delivery timelines, tracking work hours, and maintaining project forecasts.Cross-Functional Collaboration: Participate in project launch meetings, client review calls, and interdepartmental communications to drive operational excellence.Bachelor's degree or Master's degree in a scientific discipline (B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Medicine).Experience & Key Competencies: 1 to 3 years of experience in scientific writing, medical writing, or pharmaceutical CRO operations.Strong editorial, proofreading, and English grammatical skills.Ability to interpret complex clinical trial data accurately and present it concisely.Basic understanding of drug development processes and regulatory documentation standards.Proficiency with Microsoft Word formatting, document templates, and document management systems.Resume Tips for Thermo Fisher CandidatesHighlight Medical Writing & Document Types: Prominently state your 1-3 years of writing experience and specific document types handled (ICFs, Lay Summaries, Protocols) at the top of your resume.Detail Data Interpretation & QC Output: Mention metrics such as document delivery timeliness, quality audit compliance, and proficiency with MS Word templates.Add Technical Keywords: Optimize your CV with keywords like Associate Medical Writer, Scientific Writing, Informed Consent Form (ICF), Lay Summaries, cGMP, PPD, and Thermo Fisher.Q. What work model is available for this position This role offers a Hybrid / Remote work model based in Mumbai (Hiranandani Business Park). Q. What experience is required 1 to 3 years of experience in scientific writing, medical writing, or pharma/CRO operations. Q. What qualifications are eligible Bachelor's or Master's degree in a Scientific discipline (B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc). .