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Medical Writer I (Quality Check)

Syneos Health
Syneos Health
1 years
Not Disclosed
Remote
10 Feb. 17, 2026
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

Medical Writer I (Quality Check) – Remote, India | Minimum 1 Year Experience Required

Location: India (Remote)
Job ID: 25105573
Experience Required: Minimum 1 year in Medical Writing (Quality Check focus)
Employment Type: Full-Time

A leading global biopharmaceutical solutions organization is hiring a Medical Writer I (Quality Check) to support scientific and regulatory documentation through rigorous data and content quality control. This remote opportunity is ideal for early-career medical writers with hands-on experience in data integrity review, scientific content validation, and compliance-driven documentation.

This role plays a critical part in ensuring medical communication deliverables meet regulatory, scientific, and publication standards across global markets including FDA and EU jurisdictions.

Key Responsibilities

  • Perform scientific quality control (QC) of extracts, manuscripts, posters, and figure/table outputs.

  • Conduct detailed data integrity reviews to ensure accuracy and consistency across text, tables, and graphical elements.

  • Cross-check scientific content against cited references to validate medical accuracy and ensure alignment with approved product labels.

  • Ensure neutrality and balanced presentation of data in accordance with source materials.

  • Verify correct interpretation of scientific data and maintain compliance with internal style guides and journal/congress submission guidelines.

  • Ensure accurate one-to-one alignment between in-text citations and reference lists.

  • Apply AMA style guidelines and internal medical writing checklists during copyediting.

  • Maintain working knowledge of FDA, EMA, ICH, and relevant regulatory standards.

  • Participate in internal and client-facing meetings to resolve review comments and maintain timeline adherence.

  • Monitor project timelines and budgets; escalate risks to Lead Medical Writer or Project Manager when necessary.

  • Support medical writing teams in delivering high-quality, submission-ready documents.

  • Manage assigned deliverables according to SOPs and sponsor standards.

Required Qualifications

  • Bachelor’s degree in Life Sciences, Clinical Sciences, English, Journalism, or related field (preferred).

  • Minimum 1 year of experience in medical writing with a focus on quality check and data review.

  • Demonstrated experience in reviewing scientific manuscripts, abstracts, posters, and data outputs.

  • Strong understanding of scientific referencing and bibliography alignment.

  • Familiarity with AMA style guide (strongly preferred).

  • Knowledge of FDA and EU regulatory requirements; familiarity with ICH and ISO standards is an advantage.

  • Proficiency in Microsoft Word, Excel, and PowerPoint.

  • Excellent attention to detail and strong analytical skills.

  • Strong written and verbal communication skills.

  • Ability to manage multiple deadlines with minimal supervision.

  • Team-oriented mindset with strong organizational and project management skills.

About the Organization

This global biopharmaceutical solutions provider operates in over 110 countries with a workforce of approximately 29,000 professionals. Over the past five years, the organization has supported:

  • 94% of Novel FDA-approved drugs

  • 95% of EMA-authorized products

  • 200+ studies across 73,000 sites

  • 675,000+ clinical trial patients

The company is committed to diversity, inclusion, career progression, and continuous professional development. Employees benefit from structured training programs, leadership engagement, and a performance-driven environment focused on accelerating therapy delivery worldwide.

Why This Role Matters

Medical Writers specializing in Quality Check ensure scientific credibility, regulatory compliance, and publication integrity. This role directly contributes to the successful dissemination of clinical research data and regulatory documentation that supports global healthcare advancements.

Equal Opportunity Statement

The employer is committed to building a diverse, inclusive, and equitable workplace. Candidates with transferable skills are encouraged to apply. Reasonable accommodations are provided in accordance with applicable regulations.

For more verified pharma, clinical research, regulatory affairs, and medical writing opportunities, visit ThePharmaDaily.com – your global platform for pharmaceutical careers.