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Clinical Editor
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What they do
An Editor reviews stories, reports or manuscripts, makes corrections, and works with writers to improve content and structure of writing. Plans and coordinates material to be included in publications. Works with print material or website content. May specialize in copy editing (careful review of text for errors) or other types of editing; may work as an executive editor with authority to approve publications and contracts.
$94,261 / year median in Delaware
-18% projected decline
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Clinical Editor - REMOTE (EST/CST)
Wilmington, DE
Posted 3 days ago
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Day Responsibilities:
This role is responsible for managing non-clinical regulatory documents from draft through submission readiness.Key responsibilities include:
Receiving non-clinical reports from scientists and authors. Performing an initial QC review of Word documents against sources to verify accuracy, formatting to Company Style Guide, and alignment with the StartingPoint Template Conducting document formatting and ensuring compliance with company style guides. Converting text, figures, and data into the appropriate formats, including text-to-table formatting and section-by-section document review. Verifying accuracy between narrative content, tables, and figures. Performing copyediting and document standardization. Preparing documents for progression through the regulatory submission workflow. Perform the full QC review on as many of the documents that are submitted through Veeva nonclinical documentsQualifications:
BS Degree with 4 years experience directly related/carrying to document production of QC, editing, publishing. Strong working knowledge of the editorial and publishing activities within Clinical Development Regulatory document management and publishing experience. Strong QC, copyediting, and formatting skills. Experience preparing IND-supporting documents. Knowledge of bookmarks, hyperlinks, and PDF submission standards. Proficient in Microsoft Word and Adobe (creating bookmarks and internal/external hyperlinking). Toolbox (Adobe plug in), and Veeva StartingPoint template is a plus Strong collaboration skills with scientists, authors, and regulatory teams. Ability to manage high-volume workloads while maintaining quality and compliance. Strong verbal and written communication skills Job Type & Location This is a Contract position based out of Wilmington, DE. Pay and Benefits The pay range for this position is $43.00 - $47.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Wilmington,DE.