Top 531 Sr technical editor Jobs

Senior Non-Clinical Editor
Kaztronix —Wilmington, DE
- Contract
- Remote
- Microsoft Word
- Microsoft Excel
- Writing skills
Quick Apply
1d
Senior Technical Writer-Editor
Artemis Arc —Washington, DC
- $110,000 - $115,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Research
- Disability insurance
- Health insurance
Sr. Technical Writer/Editor
CSSI, Inc. —Washington, DC
- Hybrid work
- 11+ years
- English
- Senior level
Quick Apply
14d
Sr. Technical Writer - Hybrid
CEDENT —New York, NY
- Contract
- Organizational skills
- Senior level
- Communication skills
Senior Technical Writer / Editor - US CNMI
Essential Healthcare Solutions LLC —Honolulu, HI
- Military encouraged
- In-person
- Senior level
Quick Apply
Senior Writer, Editorial – Development
Stand Together —Arlington, VA
- $95,000 - $135,000 a year
- Full-time
- Senior level
- Health insurance
- Dental insurance
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Sr. Technical Writer
Rolls-Royce Power Systems AG —Mankato, MN
- $94,160 - $153,010 a year
- Full-time
- 5 years
- Office
- Analysis skills
- Paid parental leave
- Health savings account
Publications Technical Senior Editor
Honda —Alpharetta, GA
- $72,100 - $90,100 a year
- Full-time
- 5 years
- Office
- Ability to lift 50 pounds
- Paid holidays
- Loan repayment program
2d
Senior Medical Editor
Real Chemistry —Remote
- $80,000 - $95,000 a year
- Hybrid work
- Microsoft Excel
- Office
- In-person
- Paid holidays
- Health insurance
Sr. Technical Writer
Rolls-Royce —Mankato, MN
- $94,160 - $153,010 a year
- Full-time
- 5 years
- English
- Office
- Paid parental leave
- Health savings account
Senior Regulatory Writer (Temporary)
Vir Biotechnology —Remote
- $130 - $170 an hour
- Temporary
- Remote
- 7 years
- Bachelor's degree
- US work authorization
Quick Apply
Sr. Technical Writer
Fresenius Kabi —Wilson, NC
- $73,614 - $103,528 a year
- Full-time
- Senior level
- Wellness program
- Paid holidays
Sr. Technical Writer
Intone Networks —Orlando, FL
- Contract
- 3 years
- Senior level
14d
Proposal Writer Sr
PNC Financial Services Group —Pittsburgh, PA
- $63,750 - $127,500 a year
- Full-time
- Remote
- Mid-level
- Team management
- In-person
- Wellness program
- Health savings account
10d
Sr. Medical Editor (Regulatory Documents + QC) - US Home based
サイネオス・ヘルス —Morrisville, NC
- $62,000 - $108,600 a year
- Continuous improvement
- Quality control
- Mentoring
- Employee stock purchase plan
- Health insurance
Sr. Customs Entry Writer
Contingent Crew, LLC —Chicago, IL
- $34 - $36 an hour
- Full-time
- Background check
- 5 years
- Office
- Health insurance
Quick Apply
3d
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos - Clinical and Corporate - Prod —New Jersey
- $95,000 - $210,900 a year
- Full-time
- Microsoft Word
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Senior Customs Entry Writer
OEC Group —New Hyde Park, NY
- $65,000 - $75,000 a year
- Overtime
- Hybrid work
- Computer literacy
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
Senior Editor/Writer - Academic Publications
The C3 Group —Fort Belvoir, VA
- $30 - $33 an hour
- Full-time
- Microsoft Word
- Writing skills
- English
- Paid holidays
- Disability insurance
Quick Apply
11d
Senior Entry Writer/Customs Compliance
Duty Free Holding —Miami, FL
- From $85,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- 5 years
- Health insurance
- Dental insurance
Quick Apply

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Senior Non-Clinical Editor

Kaztronix -
Wilmington, DE

Quick Apply

Job Details

Contract
1 day ago

Qualifications

Microsoft Word
Communication with suppliers
Microsoft Excel
Presentation software
Clinical development
Writing skills
Word embeddings
Visio
Pharmaceutical company experience
Vendor relationship management
Vendor communication
Content publishing

Full Job Description

Job Summary
This position is responsible for overall quality control (QC) review and submission-ready publishing of nonclinical documents. The Senior Nonclinical Editor will copyedit/proofread, format, and perform internal consistency review of document content in accordance with company SOPs and processes to ensure documents meet required standards. This role will support all documents written by authors from Drug Metabolism and Biopharmaceutics (DMB), Chemistry Manufacturing and Controls (CMC), Toxicology (Tox), and Translational Sciences. This position may also assist in clinical document QC and publishing tasks when appropriate to meet submission timelines. The Senior Nonclinical Editor performs the activities with minimal oversight needed.

Summary of the Essential Functions of the Job

Perform internal document QC review of nonclinical documents (eg, DMB, CMC, TOX, TRS, PRECLIN) to ensure compliance with the Style Guide, template formatting, and submission ready standards.
Copyedit/proofread for grammar, style, and formatting according to AMA and style guides.
Ensure internal consistency and confirm that data are reported correctly, statements accurately reflect a common message and text to tables, figures, and appendices are accurate and consistently presented.
Check the reference list in documents, including verifying citation information via PubMed, ordering copies of references, and adding to the electronic document management system (EDMS), and ensuring each reference is cross-referenced in the document.
Proofread documents against the standard templates to ensure compliance with required sections and text.
Perform publishing of PDF documents to submission-ready standards. May involve multiple document compilation of PDF files to include appendices.
Assist Medical Writing Operations staff with clinical document QC and publishing, as appropriate.
Participate in process improvement initiatives and support Medical Writing staff with other tasks, as appropriate.
May interact cross-functionally to support clinical and nonclinical processes and template updates.

Minimum Requirements

Bachelor s degree in English, Basic Science, Business, or other analytical field with 4 years related experience in the pharmaceutical industry OR 8+ years of experience in a discipline directly related to document production (eg, medical writing, QC, editing, publishing).
Strong working knowledge of the editorial and publishing activities within Clinical Development.
Proficient in Microsoft Word, including the ability to format tables, insert cross-references, apply styles, and use templates. Experience with PowerPoint, Excel, Visio, Adobe.
Strong working knowledge of Adobe PDF bookmarking and internal/external hyperlinking to meet submission-ready standards.
Experience in the use of an EDMS (eg, Veeva Vault or SharePoint).
Ability to effectively communicate with vendors and manage outsourced editorial work.
Keen attention to detail.
Ability to manage multiple activities, prioritize effectively, and work in a fast-paced, deadline-driven environment.
Strong organizational and time management skills.
Strong verbal, written, and interpersonal communication skills.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.

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