Senior Medical Writer – Abstracts & Manuscripts (Remote)
Location: India – Remote
Job Type: Full-Time
Job ID: 25104370
Updated: December 24, 2025
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We transform clinical, medical affairs, and commercial insights into actionable outcomes that meet modern healthcare and market demands.
With a presence in 110 countries and over 29,000 employees, Syneos Health provides a collaborative and innovative environment that empowers employees to deliver meaningful impact in clinical development, patient care, and regulatory excellence.
Position Overview
We are seeking a Senior Medical Writer to lead the creation of high-quality scientific documents including journal manuscripts, abstracts, posters, and client presentations. The role involves mentoring junior writers, coordinating cross-functional inputs, ensuring regulatory compliance, and delivering projects efficiently, on-time, and within budget.
Key Responsibilities
Medical Writing & Project Leadership:
Lead and manage medical writing projects for assigned studies or regulatory submissions.
Author, review, and finalize clinical manuscripts, abstracts, posters, and internal/external presentations.
Review statistical analysis plans, tables, listings, and figures for accuracy, consistency, and clarity.
Identify and resolve writing-related issues, escalating where necessary.
Ensure projects meet quality standards, deadlines, and budget expectations.
Collaboration & Mentorship:
Mentor and guide junior medical writers on complex projects.
Work closely with Biostatistics, Data Management, Regulatory Affairs, and Medical Affairs teams to ensure accuracy and completeness of deliverables.
Serve as a peer reviewer, providing constructive feedback to team members.
Regulatory & Compliance:
Adhere to journal, congress, regulatory, and internal company guidelines.
Ensure compliance with company SOPs, templates, and client-specific standards.
Conduct literature searches to support evidence-based writing.
Technical Skills & Tools:
Proficiency in figure-creation and data visualization tools such as GraphPad Prism and Adobe Illustrator.
Familiarity with publication planning software, e.g., Datavision.
Strong command of MS Office (Word, Excel, PowerPoint, Outlook).
Additional Responsibilities:
Maintain awareness of project budgets and communicate deviations.
Complete administrative and documentation tasks within specified timeframes.
Minimal travel required (<25%).
Required Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field.
Proven experience as a medical writer in clinical research, regulatory, or medical communications.
Ability to lead projects and mentor junior writers.
Strong understanding of clinical trial data, regulatory requirements, and publication guidelines.
Excellent written, verbal, and interpersonal communication skills.
Strong organizational skills, attention to detail, and ability to manage multiple priorities.
Why Join Syneos Health
Contribute to global clinical and regulatory projects with real-world impact.
Collaborate with diverse, cross-functional teams in a supportive, innovative environment.
Access continuous career development, mentorship, and technical training.
Work on cutting-edge therapies that improve patient outcomes worldwide.
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