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Writer Author Jobs (NOW HIRING)

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142.10K - $195.36K/yr

The ideal candidate is a hands-on writer who spends the majority of their time authoring and developing scientific and regulatory documents rather than primarily editing or managing teams. Strong ...

BioFire Diagnostics

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

... policies Review author disclosures, acknowledgments, and contribution statements to ensure ... Written Communications - including the ability to communicate technical data in written form

Lancesoft

Technical Writer

Foster City, CA · On-site

$55 - $57/hr

The technical writing contractor for BaseOps will author and maintain all types of BaseOps technical documentation to support technicians and engineers with maintaining our autonomous vehicle fleet.

bioMérieux

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

Ability to collaborate with and oversee external vendors, authors, and contributors, ensuring ... writing at the time of the offer. In addition, bioMérieux offers a competitive Total Rewards ...

Staffingine LLC

CMC Writer

Paramus, NJ · On-site

CMC Writer Job Location: Paramus, NJ Job Type: Contract ... Authors a range of clinical documents, including regulatory documents following defined templates ...

Kohler Co.

Technical Writer

Kohler, WI · On-site

$63.90K - $95.90K/yr

Technical Writer Work Mode: Onsite Location: Onsite - Kohler, WI Opportunity Responsible for the ... Experience authoring within a tagged language * Authoring experience in XML/DITA * Experience ...

Kohler

Technical Writer

Kohler, WI

$63.90K - $95.90K/yr

Technical Writer Work Mode: Onsite Location:  Onsite - Kohler, WI Opportunity Responsible for the ... Experience authoring within a tagged language * Authoring experience in XML/DITA * Experience ...

Volto Consulting

Technical Writer

Alpharetta, GA

Technical Writer Skills: Siebel CRM Technical System Administration (Windows and Unix), Technical ... Uses advanced authoring tools to draft essential user documentation; Employs advanced organization ...

Cypress HCM

Technical Writer

Santa Clara, CA

$65 - $82.39/hr

Technical Writer The Digital Experiences team is seeking a Technical Writer to join our team. This ... Experience with DITA CCMS authoring - Heretto CCMS * Experience with Oxygen XML Editor, and ...

Global Channel Management, Inc.

Tech Writer

Andover, MA · On-site

$45/hr

Author technical report summarizing production, laboratory, validation activities and associated data ?Collate and compile data report, data sheet, and/or database from paper-based and electronic ...

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How much do writer author jobs pay per hour?

As of May 31, 2026, the average hourly pay for writer author in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What does a Writer Author do?

A Writer Author creates written content for various mediums, such as books, articles, blogs, scripts, or marketing materials. They research topics, develop ideas, and craft engaging narratives or informative pieces tailored to their audience. Some writers work independently, while others collaborate with publishers, editors, or clients. Strong writing skills, creativity, and attention to detail are essential for success in this field.

What are the key skills and qualifications needed to thrive in the Writer Author position, and why are they important?

To thrive as a Writer Author, you need exceptional writing, grammar, storytelling, and research skills, typically developed through a degree in English, communications, journalism, or a related field. Familiarity with word processing software, content management systems, and sometimes publishing or editing tools is often required. Creativity, self-motivation, strong time management, and attention to detail are important soft skills that set successful authors apart. These qualities are vital for consistently producing high-quality content, meeting deadlines, and effectively engaging targeted audiences.

What are typical daily responsibilities for a Writer Author?

Daily responsibilities for a Writer Author often include researching topics, drafting and revising manuscripts or articles, and collaborating with editors or clients to refine content. Many writers also allocate time for brainstorming new ideas, conducting interviews, and fact-checking to ensure the accuracy of their work. Additionally, Writer Authors may spend part of their day managing their writing schedule, submitting work to publishers, and networking with other industry professionals. The role often requires self-motivation, adaptability, and excellent organizational skills to handle multiple assignments or projects simultaneously.
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Writer Author jobs near you
Infographic showing various Writer Author job openings in the United States as of May 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Senior Medical Writer

Ambition 24Hours Inc

The Lakes, NV • Remote

$142.10K - $195.36K/yr

Contractor

Posted 9 days ago

Job description

Senior Medical Writer – Full-Time Remote Opportunity

───────────────────────────
Location: Fully Remote (U.S.)
Industry: Pharmaceutical / Biotechnology
Employment Type: Full-Time
Salary Range: $142,100 – $195,360 annually
Experience Level: Mid-Senior
───────────────────────────

Job Overview
───────────────────────────
We are seeking an experienced Senior Medical Writer to support clinical development and regulatory documentation activities within a leading biotechnology environment. This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive experience authoring Clinical Study Reports (CSRs), protocols, and regulatory submission documents across Phase I–III studies.

The ideal candidate is a hands-on writer who spends the majority of their time authoring and developing scientific and regulatory documents rather than primarily editing or managing teams. Strong expertise in clinical development, regulatory writing standards, and cross-functional collaboration is essential.

───────────────────────────
Key Responsibilities
───────────────────────────
Author and edit clinical study documents including protocols, protocol amendments, informed consent forms, and Clinical Study Reports (CSRs)
Prepare regulatory submission documents including briefing books and eCTD summaries/modules
Draft aggregate safety and efficacy documents including DSURs, PBRERs, and Investigator Brochures
Manage document timelines, review cycles, and comment adjudication processes
Lead and facilitate document-related meetings with cross-functional study teams
Collaborate with clinical, biostatistics, regulatory, pharmacovigilance, and data management teams
Interpret and present complex clinical data in clear scientific narratives, tables, and graphics
Ensure all documentation complies with regulatory guidelines, industry standards, and internal style guides
Support process improvements, templates, and standard operating procedures within Medical Writing

───────────────────────────
Requirements
───────────────────────────
Bachelor’s degree or higher in a scientific discipline required
7–10+ years of medical writing experience within biotech, pharmaceutical, or CRO environments
Extensive experience authoring Clinical Study Reports (CSRs) and protocol amendments required
Experience with INDs, NDAs, BLAs, DSURs, PBRERs, and regulatory briefing books strongly preferred
Strong understanding of clinical development processes and regulatory requirements
Experience with eCTD submissions and Modules 2–5 preferred
Ability to interpret complex clinical and statistical data
Excellent scientific writing, communication, and organizational skills
Proficiency with Microsoft Office Suite, Adobe Acrobat, Veeva, SharePoint, or similar document management systems
Ability to manage multiple projects and work independently in a remote environment

───────────────────────────
Ideal Candidate Profile
───────────────────────────
Highly experienced clinical medical writer with strong Phase I–III study expertise
Focused primarily on authoring scientific and regulatory content rather than editing or project management
Demonstrated excellence in CSR development and clinical science documentation
Biotech or pharmaceutical industry background strongly preferred
CRO experience considered
Strong attention to detail with the ability to meet strict timelines and regulatory standards