Medical Writer I – Quality Check (Scientific & Data QC)
Job ID: 25105573
Location: Gurugram, India (Hybrid)
Employment Type: Full-Time
Company: Syneos Health
Job Overview
Syneos Health is hiring a Medical Writer I (Quality Check) to support scientific quality control, data integrity review, and editorial excellence across medical writing deliverables. This hybrid role in Gurugram is designed for professionals with experience in medical writing and scientific content QC, particularly in regulatory, publication, and promotional materials within the pharmaceutical or biotechnology sector.
The selected candidate will ensure accuracy, consistency, regulatory compliance, and alignment with global guidelines across manuscripts, abstracts, posters, extracts, and figure/table outputs.
Experience Required
Minimum 1 year of medical writing experience
Proven experience in scientific data and content quality control (QC) review
Experience reviewing manuscripts, abstracts, posters, extracts, and figure/table outputs
Familiarity with global regulatory guidelines (FDA, EMA, ICH) preferred
Exposure to regulatory and publication-focused deliverables in pharma/biotech environment
Educational Qualifications
Bachelor’s degree (preferred) in Life Sciences, Clinical Sciences, English, Journalism, or related field
Relevant experience in copyediting, publishing, or data integrity review may be considered
Key Responsibilities
Scientific Data & Content Quality Review
Conduct comprehensive data integrity reviews to ensure consistency across text, tables, and figures
Cross-check scientific content against cited references for medical accuracy and neutrality
Verify correct interpretation of clinical and scientific data
Ensure alignment with approved product labeling and regulatory guidance
Confirm accurate in-text citations with one-to-one reference list alignment
Regulatory & Guideline Compliance
Ensure compliance with FDA, EMA, ICH, and applicable industry standards
Maintain familiarity with regulatory document requirements and scientific publication guidelines
Align formatting and structure with internal style guides and journal/congress-specific standards
Apply American Medical Association (AMA) style or custom style guidelines as required
Editorial & Project Support
Copyedit documents for grammar, punctuation, clarity, and consistency
Review extracts, manuscripts, posters, and figure/table outputs for scientific QC
Monitor timelines and budgets for assigned projects and proactively flag risks
Participate in internal and client-facing meetings to resolve comments and ensure timely delivery
Support the Lead Medical Writer and Project Manager with progress updates
Manage deliverables according to SOPs and client standards
Core Competencies
Strong attention to detail and scientific accuracy
Expertise in data QC and content alignment
Excellent written and verbal communication skills
Strong project management and organizational abilities
Ability to manage multiple assignments under strict deadlines
Proficiency in Microsoft Word, Excel, and PowerPoint
Ability to work independently and collaboratively within cross-functional teams
Preferred Knowledge
Familiarity with FDA and EU regulatory requirements
Understanding of ICH guidelines and ISO standards relevant to regulatory documentation
Experience working within clinical development, regulatory writing, or medical communications
About Syneos Health
Syneos Health is a global biopharmaceutical solutions organization providing integrated clinical, medical affairs, and commercial services. With operations across more than 110 countries, the company supports pharmaceutical and biotechnology clients in accelerating therapy development and regulatory approval.
Over the past five years, Syneos Health has supported the development of the majority of newly approved FDA and EMA therapies, reinforcing its leadership in clinical research and medical writing excellence.
Why Join Syneos Health?
Opportunity to work on high-impact regulatory and scientific deliverables
Structured career development within medical writing and clinical documentation
Exposure to global regulatory frameworks and publication standards
Collaborative, compliance-driven, and performance-oriented work culture
This Medical Writer I (Quality Check) role in Gurugram is ideal for early-career medical writing professionals seeking to strengthen their expertise in scientific QC review, regulatory compliance, and publication-quality documentation within the global pharmaceutical industry.
Apply now through The Pharma Daily to explore medical writing and regulatory documentation careers with leading biopharmaceutical organizations.
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