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Medical Writer Ii (Clinical Trial Transparency)

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 May 5, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Job Title: Medical Writer II (Clinical Trial Transparency)

Job Location: India - Asia Pacific - Home-Based


Company Overview

Syneos Health is a leading integrated biopharmaceutical solutions organization that accelerates customer success by transforming clinical, medical affairs, and commercial insights into actionable outcomes. The company operates in 110 countries with a mission to bring customers and patients at the center of everything they do.


Role Summary

As a Medical Writer II, you will be responsible for producing a variety of clinical and regulatory documents including clinical study protocols, reports, patient narratives, and investigator brochures. You will work with cross-functional teams, adhering to regulatory standards and ensuring high-quality content.


Key Responsibilities

  • Mentor less experienced medical writers and support them on projects.

  • Develop, write, and edit medical writing deliverables including:

    • Clinical study protocols and amendments

    • Clinical study reports

    • Patient narratives

    • Annual reports

    • Investigator brochures

  • Review statistical analysis plans and table/figure/listing specifications.

  • Collaborate with data management, biostatistics, regulatory affairs, and medical affairs teams to produce high-quality deliverables.

  • Serve as a peer reviewer, ensuring scientific content, clarity, consistency, and proper formatting.

  • Ensure adherence to regulatory standards like ICH-E3, SOPs, client standards, and approved templates.

  • Conduct online clinical literature searches when required.

  • Maintain a good understanding of the drug development process and regulatory guidelines.

  • Manage project budgets, working within the allocated hours and communicating any changes.

  • Complete administrative tasks in a timely manner.

  • Minimal travel may be required (less than 25%).


Qualifications

Required

  • Education:

    • Bachelor of Science with relevant writing experience or Bachelor of Arts in Social Sciences, English, Communications, or related fields, with relevant scientific/medical knowledge.

  • Experience:

    • Strong understanding of English grammar, FDA/ICH regulations, and AMA style guide.

    • Ability to interpret and present clinical data.

    • Strong proficiency in Microsoft Word, Excel, PowerPoint, and email.

    • Excellent presentation, proofreading, and leadership skills.


Work Environment

Syneos Health fosters a Total Self culture, where employees are encouraged to be their authentic selves. The company provides career development opportunities, technical and therapeutic area training, and a peer recognition program.


How to Apply

Interested candidates can apply through the Syneos Health career portal.