Medical Editor II (Quality Check) – Full-Time, On-Site (Pune, MH, India)
Job ID: 25105257
Updated: Today
Overview:
Syneos Health®, a global leader in integrated biopharmaceutical solutions, is seeking a Medical Editor II (Quality Check) to ensure the accuracy, integrity, and compliance of medical writing deliverables. This role focuses on data and content quality control (QC), reviewing manuscripts, posters, figures, tables, and regulatory documents to meet internal, sponsor, and industry standards.
Experience Level: Mid-Level – Minimum 1–2 years of medical editing or scientific QC experience in pharmaceutical, clinical, or biopharmaceutical environments.
Key Responsibilities:
Perform data integrity reviews of assigned documents, ensuring accuracy across text, tables, figures, and references.
Verify alignment of content with approved product labels, source material, and internal/external guidelines.
Cross-check scientific content for medical/scientific accuracy, neutrality, and consistency.
Ensure proper citation alignment between in-text references and reference lists.
Maintain familiarity with FDA, EU, ICH, and other regulatory requirements relevant to medical writing deliverables.
Copyedit documents according to AMA style guidelines or client-specific styles, including grammar, punctuation, formatting, and structure.
Collaborate with internal teams and clients to resolve comments, meet deadlines, and ensure quality deliverables.
Track timelines and budgets for assigned projects, updating the Lead Medical Writer or Project Manager as required.
Participate in document compilation, publishing, and management to support client submissions.
Essential Requirements:
Bachelor’s degree in Life Sciences, Clinical Sciences, English, Journalism, or related field; equivalent experience considered.
Minimum 1–2 years of Medical Editing or Scientific QC experience.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Strong attention to detail, problem-solving, and organizational skills.
Excellent written and oral communication skills, with the ability to work independently and in a team environment.
Desired Skills & Qualifications:
Familiarity with AMA style guide and medical writing best practices.
Understanding of FDA, EU, ICH, and ISO requirements for regulatory documents.
Experience reviewing scientific manuscripts, posters, tables/figures, and regulatory extracts.
Ability to manage multiple assignments simultaneously and meet strict deadlines.
Why Join Syneos Health:
Work with a global leader involved in 94% of Novel FDA Approved Drugs and 95% of EMA Authorized Products.
Join a diverse, inclusive, and collaborative culture that encourages Total Self authenticity.
Opportunities for professional development, training, and career progression in a dynamic, innovative environment.
Contribute to medical writing deliverables that directly support clinical research, regulatory submissions, and global patient outcomes.
Additional Details:
Location: On-site in Pune, MH, India
Employment Type: Full-Time
Tasks may evolve; equivalent experience, skills, and education may be considered.
Syneos Health is committed to diversity, inclusion, and compliance with the Americans with Disabilities Act, including reasonable accommodations.
Global Impact:
At Syneos Health, work here matters everywhere. Join a team dedicated to delivering high-quality medical writing outputs that support clinical development, regulatory compliance, and patient care worldwide.
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