ZipRecruiter

Log In

1

Senior Content Writing Jobs in Delaware (NOW HIRING)

Troutman Pepper

Senior Pricing Analyst

Wilmington, DE · Hybrid

Superior interpersonal and communication skills, both oral and written. * Sound professional acumen ... This position description is intended to describe the general content of and requirements for the ...

Dlapiper

Digital Marketing Coordinator

Wilmington, DE · On-site +1

$30.99 - $48.35/hr

... Senior Manager, Communications, the Digital Marketing Coordinator works closely with internal ... Publish firm content within the employee advocacy tool * Resize or crop digital images using image ...

Pj Fitzpatrick

Exterior Remodeling trainer

New Castle, DE

$31.50 - $42/hr

The trainer also supports standardized curriculum, digital learning content, and training resources ... Partner with Senior Full Line Technical Trainer to identify skill gaps and improve employee ...

previous pagenext page

Showing results 21-40

All JobsContent Writing JobsSenior Content Writing JobsSenior Content Writing Jobs in Delaware

Senior Content Writing information

What is the difference between Senior Content Writing vs Content Strategist?

AspectSenior Content WritingContent Strategist
Required CredentialsTypically a bachelor’s degree in English, Journalism, or related field; strong writing portfolioOften a bachelor’s degree in Marketing, Communications, or related; experience in content planning
Work EnvironmentCreates content, writes articles, blogs, and web copy; often independently or in small teamsDevelops content plans, oversees content projects, collaborates with marketing teams
Industry UsageUsed across digital marketing, publishing, and media companiesCommon in marketing agencies, corporate marketing departments, and media firms

While Senior Content Writers focus on creating high-quality content, Content Strategists develop overall content plans and strategies. Both roles require strong writing skills, but Content Strategists have a broader focus on planning and coordination, making them complementary roles within content teams.

Are senior content writers still in demand?

Senior content writers remain in demand as companies prioritize high-quality content for marketing, SEO, and brand engagement. They often require strong writing skills, SEO knowledge, and familiarity with content management systems, making experienced writers valuable across industries.

What are the key skills and qualifications needed to thrive as a senior content writer, and why are they important?

To thrive as a Senior Content Writer, you need advanced writing, editing, and research skills, typically supported by a degree in English, communications, or a related field. Familiarity with content management systems (CMS), SEO tools like SEMrush or Ahrefs, and analytics platforms is essential. Outstanding creativity, collaboration, and time management abilities help you produce high-quality content while meeting deadlines and adapting to brand voice. These skills ensure impactful, engaging content that drives audience engagement and supports organizational goals.

What is a senior content writer?

A Senior Content Writer is an experienced professional responsible for creating, editing, and managing high-quality written content for various platforms, such as websites, blogs, and marketing materials. They often lead content projects, develop content strategies, and mentor junior writers. Senior Content Writers possess strong writing, research, and communication skills and have a deep understanding of target audiences and SEO best practices. Their work helps establish a brand’s voice and supports overall business goals.

How does a senior content writer typically collaborate with other departments within a company?

Senior Content Writers frequently work closely with marketing, design, SEO, and product teams to ensure content aligns with overarching business goals. Collaboration often involves participating in brainstorming sessions, providing content briefs, and adapting writing based on feedback from stakeholders. This cross-functional teamwork helps ensure messaging consistency, supports campaign objectives, and enhances user experience. Effective communication and project management skills are essential to balance input from multiple sources and meet deadlines.
What are the most commonly searched types of Content Writing jobs in Delaware? The most popular types of Content Writing jobs in Delaware are:
What are popular job titles related to Senior Content Writing jobs in Delaware? For Senior Content Writing jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Senior Content Writing jobs in Delaware look for? The top searched job categories for Senior Content Writing jobs in Delaware are:
What cities in Delaware are hiring for Senior Content Writing jobs? Cities in Delaware with the most Senior Content Writing job openings:
Senior Content Writing jobs near you

Senior Manager, Regulatory Operations

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted 3 days ago

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
The job is based in Wilmington Delaware, US. (Minimum 3 days per week in the office. Local candidates or those willing to relocate only).
Job Summary (Primary function)
The Senior Manager, Regulatory Operations, is responsible for managing and maintaining existing development and marketing authorization dossiers, managing RIM objects and compiling submissions in compliance with ICH specifications and Health Authority regulations globally. The Sr Manager will coordinate with functional leads in various disciplines to ensure compliant documents, maintain regulatory information and the physical and electronic regulatory archives, mentor on eCTD requirements and other duties and/or special projects as assigned or required.
Essential Functions of the Job (Key responsibilities)
  • Responsible for the timely planning, compiling, publishing, review and delivery of compliant regulatory submissions to Regulatory Health Authorities.
  • Ensures documents and RIM objects comply with submission ready standards and guidelines and provides guidance with respect to requirements.
  • Maintains and archives all regulatory correspondence in appropriate systems.
  • Liaises with vendors for submission support, as needed.
  • Participates in validation or verification testing of templates, electronic document management system, information management and document/submission publishing related tools.
  • Maintains tracking tools and systems for regulatory information, including submission content plans.
  • Support other areas of the company (eg., Business Development) concerning regulatory documentation, as needed.
  • Maintains current working instructions for regulatory-related systems (e.g. publishing software, RIM and EDMS.
  • Mentors team members on submission processes and requirements and may manage contract Regulatory Operations personnel.
  • Contribute positively to a strong culture of business integrity and ethics.
  • Act within compliance and legal requirements as well as within company guidelines.
  • Coordinate the preparation and review of documents for regulatory submissions (e.g. cover letters, forms, DSURs, safety reports, etc.).
  • Participates in the preparation of dossiers containing manufacturing, preclinical, and clinical data.
  • Provides guidance to authors for clear document and data presentation and location in order to optimize submission navigation as well as the regulatory review and approval process.

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Bachelor's degree in a relevant field (e.g., science, technology, health, or business management) or equivalent experience. Candidates with diverse educational backgrounds are encouraged to apply.
  • Minimum of relevant experience in a regulatory affairs environment with document management systems, electronic publishing systems, and electronic submissions, including eCTD, and direct submission to global Health Authorities. Candidates with equivalent skills and knowledge are encouraged to apply.
  • Experience in drug development and familiarity with global regulatory submission content and formats.
  • Experience with SPL, advertising and promotional submissions, device submissions, and combination products submissions is valued.
  • Strong technical knowledge and proficiency in publishing and related computer software, including advanced word processing and design tools such as MS Word, Adobe, and Adobe plug-ins.
  • Strong organizational, communication, and writing skills are essential.
  • Ability to manage multiple priorities and projects, with support for diverse working styles and needs.
  • Strong attention to detail and quality.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
vwd

Apply