# Senior Medical Editor (QC and Regulatory Editing)

**Company**: Syneos Health
**Location**: IND-Hyderabad-Hybrid
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/IND-Hyderabad-Hybrid/Senior-Medical-Editor--QC-and-Regulatory-Editing-_25113892-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_ee1242b8-ed4

## Description

Syneos Health is seeking a Senior Medical Editor (QC and Regulatory Editing) to join their team.

As a Senior Medical Editor, you will maintain strong familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure that documents meet or exceed sponsor and regulatory requirements and guidance.

Responsibilities:

- Represent the editorial group in medical writing, on study teams, and in cross-departmental project teams as needed.

- Monitor timelines and budgets for assigned projects and update the lead medical writer, project manager, and/or direct supervisor if deliverables are at risk.

- Provide technical support and expertise as appropriate, conduct training of medical editing staff, and function as a mentor.

- Serve as project lead for deliverables of assigned complex and/or large medical writing projects.

- Copyedit assigned documents, applying correct grammar, punctuation, spelling, and style following AMA Manual of Style or various custom style guidelines.

- Perform quality review of assigned documents to ensure accuracy.

- Contribute to the development of process improvement tools and the development or revision of internal policies and procedures affecting editorial work.

Education Requirements:

- 4 Year/Bachelor’s degree in the life sciences, clinical sciences, or English/journalism; or relevant copyediting and/or quality review experience.

Additional Qualifications:

- 3-5 years of copyediting experience; pharmaceutical/medical device or contract research organization experience preferred.

- Strong proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint).

- Excellent attention to detail, including strong copyediting, quality review, accuracy, problem solving, organizational, interpersonal, presentation, project management, and team-oriented skills.

- Knowledge of FDA and EU requirements, ICH regulations, and ISO standards as applicable to regulatory documents required.

## Skills

### Required
- Microsoft Office Suite
- AMA Manual of Style
- FDA and EU requirements
- ICH regulations
- ISO standards
- copyediting
- quality review
- project management

### Nice to have
- pharmaceutical/medical device experience
- contract research organization experience

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/IND-Hyderabad-Hybrid/Senior-Medical-Editor--QC-and-Regulatory-Editing-_25113892-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)