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Medical Writer- Future Roles (India)

Syneos Health
Syneos Health
3-5 years
upto 7 LPA
Remote, India, India
10 April 30, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate 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

Medical Writer – Future Opportunities (India)

Location: India (Remote)
Job Type: Full-Time
Company: Syneos Health
Experience Required: 3–5 Years
Freshers Eligible: No
Job Requisition ID: 25107322


About the Company

Syneos Health is a globally recognized biopharmaceutical solutions company focused on accelerating customer success across clinical development, medical affairs, and commercialization. Operating in more than 110 countries with over 29,000 professionals worldwide, the organization supports pharmaceutical, biotechnology, and healthcare innovators in bringing therapies from laboratory to patient care efficiently and effectively.

The company is known for its strong presence in clinical research, regulatory operations, pharmacovigilance, medical writing, and drug development services globally.


Job Overview

Syneos Health is building a talent pipeline for future Medical Writer opportunities in India. This remote role is ideal for experienced medical writing professionals with strong scientific communication skills, regulatory writing expertise, and experience within the pharmaceutical, biotechnology, medical device, or CRO industry.

The selected candidate will contribute to the development of high-quality clinical and regulatory documents while collaborating with cross-functional global teams including biostatistics, regulatory affairs, clinical operations, pharmacovigilance, and medical affairs.

This is not an active immediate opening but an opportunity to be considered for upcoming hiring requirements.


Key Responsibilities

  • Prepare and manage a wide range of clinical and regulatory medical writing deliverables with scientific accuracy and regulatory compliance

  • Develop documents such as Clinical Study Protocols, Clinical Study Reports (CSRs), Investigator Brochures, IND submissions, NDA submissions, patient narratives, safety reports, informed consent forms, annual reports, and plain language summaries

  • Support scientific publications including journal manuscripts, abstracts, posters, and conference presentations

  • Ensure adherence to ICH guidelines, FDA regulations, GCP standards, company SOPs, and approved templates

  • Coordinate document review cycles, editorial reviews, and quality control processes

  • Perform literature reviews and scientific data analysis to support medical documentation

  • Collaborate with internal stakeholders including Data Management, Biostatistics, Regulatory Affairs, Pharmacovigilance, and Medical Affairs teams

  • Review statistical analysis plans, tables, figures, and listings for consistency and scientific relevance

  • Mentor junior medical writers and contribute to process improvement initiatives within the medical writing department

  • Maintain timelines, quality standards, and budget expectations for assigned projects


Required Qualifications

  • Bachelor’s, Master’s, PharmD, MD, PhD, or equivalent degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or related healthcare disciplines

  • 3–5 years of professional experience in medical writing, regulatory writing, or scientific writing

  • Prior experience in pharmaceutical companies, biotechnology organizations, medical device companies, or CROs is mandatory

  • Strong understanding of FDA regulations, ICH guidelines, GCP standards, and publication practices

  • Experience preparing clinical and regulatory documents for global submissions

  • Excellent scientific writing, English grammar, editing, and communication skills

  • Familiarity with AMA Manual of Style and scientific publication standards preferred


Why Professionals Prefer Syneos Health

  • Global exposure to clinical research and regulatory projects

  • Remote work flexibility within India

  • Opportunity to work with leading pharmaceutical and biotechnology sponsors

  • Strong career development and learning environment

  • Collaborative and diverse global work culture

  • Involvement in cutting-edge drug development programs


Important Note for Applicants

This opportunity is designed for experienced medical writing professionals only. Freshers and candidates without prior industry exposure in medical writing or clinical regulatory documentation may not be eligible for consideration.

Applicants expressing interest may be added to the company’s future talent pipeline for upcoming Medical Writer openings across India.


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