Medical Editor at Syneos Health, Apply Now!
Looking to make a real impact in the world of clinical research and regulatory writing? Syneos Health, a global biopharmaceutical solutions leader, is hiring a Senior Medical Editor (Regulatory) in Pune. If you’re skilled in AMA style, FDA/EU guidelines, and medical writing standards, this full-time opportunity allows you to work in a supportive, collaborative, and innovation-driven environment—where your expertise accelerates life-changing therapies to market.
About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE.
Job Description for Sr Medical Editor
Location: Pune
Job ID: 25002456
Why Syneos Health:
- Passionate about developing our people
- Committed to Total Self culture as Sr Medical Editor
- Building a company where diversity is celebrated
Job Responsibilities
Key Responsibilities include:
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Maintain familiarity with FDA, EU, and other relevant guidelines and industry standards
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Represent the editorial group in Medical Writing and cross-functional teams
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Monitor project timelines and budgets; provide updates to leadership
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Provide technical expertise and mentorship to medical editors
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Lead complex medical writing projects and coordinate internal meetings
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Copyedit documents with AMA or custom style guides as Sr Medical Editor
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Conduct data integrity review
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Support process improvements and SOP development
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Compile and publish medical writing deliverables as needed
Qualifications
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Bachelor’s degree (preferred) in life sciences, clinical sciences, or English/journalism
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Significant copyediting and publishing experience preferred for Sr Medical Editor
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Proficiency in Microsoft Office; Adobe Acrobat or markup language preferred
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Excellent attention to detail and strong editorial skills
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Strong understanding of AMA style guide
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Knowledge of FDA/EU/ICH/ISO guidelines is preferred
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Ability to multitask and work independently or in teams
About Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.
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