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Science Writer Jobs Near Me

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred) * 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas * Proven ...

Deep knowledge of life science including cells, genetics, and ecosystems, earth science including ... and writing lab reports. Emphasizes hands-on investigation and critical thinking, connecting ...

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

Prepares, writes, and edits content for items such as RFPs, RFQs, RFIs, and grants. * Gathers information from client websites. Distributes and creates a timeline for completion.

... and writing recursive methods. Emphasizes developing computational thinking and problem ... Familiar with AP Computer Science A curriculum across ten units and common challenges such as ...

Guides students through designing experiments, analyzing quantitative data, writing laboratory reports, and applying scientific reasoning to real-world problems. Emphasizes connecting theory to ...

Content Writer (Remote) Wing is on the exciting mission of redefining the future of work for companies worldwide! We are looking to be the one-stop shop for companies that are looking to build world ...

Strong communication skills: both written and spoken. Work with Application Team members to enhance their understanding of end-user and technical documentation. Ensure messages and terminology is ...

Content Writer (Remote) Wing is on the exciting mission of redefining the future of work for companies worldwide! We are looking to be the one-stop shop for companies that are looking to build world ...

Job Title Location 3727 Park Mill Run Drive, Hilliard, OH, 43026, United States Job Category Service - Management/Admin Employee Type Non-Exempt FT Contact information Name Elizabeth M Motter Phone ...

Description Assist the service manager in maintaining accurate and on-time reports and records relative to the service department's operation within the dealership. Job Duties : * Fields internal and ...

Description Assist the service manager in maintaining accurate and on-time reports and records relative to the service department's operation within the dealership. Job Duties : * Fields internal and ...

Automotive Service Writer

Columbus, OH · On-site

$48K - $75K/yr

Alpha Automotive is looking for an Automotive Service Writer to join our rapidly growing team! Here at Alpha Automotive, we pride ourselves on providing the best service possible for our customers by ...

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Science Writer information

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$70.5K

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How much do science writer jobs pay per year?

As of Jun 26, 2026, the average yearly pay for science writer in the United States is $70,499.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,000.00 and $74,000.00 per year, depending on experience, location, and employer.
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What are the most commonly searched types of Science Writer jobs? The most popular types of Science Writer jobs are:
Who are the top companies hiring for Science Writer jobs? The top 10 employers for Science Writer jobs are:
A map of the United States highlighting the number of Science Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Science Writer job openings in each state, with California having the most at 2 and Hawaii the least at 0.
Lead Medical Writer

Lead Medical Writer

Medasource

Dublin, OH • On-site

$80 - $90/hr

Contractor

Posted 5 days ago


Job description

Lead Medical Writer
Remote (must be based in EST)
Compensation: $80-$90 per hour
Contract Length: 2 month Contract to Hire (40 hours/week)
Start Date: 7/1/26
ABOUT THE ROLE
Our client is a global healthcare services and products company providing pharmaceuticals, medical products, and supply chain solutions to hospitals, pharmacies, and healthcare providers. The organization plays a critical role in helping healthcare systems improve efficiency, reduce costs, and enhance patient care through integrated distribution and data-driven solutions. As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and responses to health authority queries. You will contribute scientifically and strategically to submission teams, plan data analyses, review statistical analysis plans, and collaborate with cross-functional stakeholders such as Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs. This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates must be available to work in the Eastern Standard Time zone.
WHAT YOU'LL DO
  • Autonomously write and review clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and other regulatory submissions such as responses to health authority questions, briefing books, 120-day safety updates, pediatric investigational plans, and investigator brochures
  • Contribute scientifically and strategically to submission teams at the project and/or study team level, providing input on pooling strategy, content expertise, and guidance on regulatory requirements
  • Plan and review data analyses and presentations for CSRs; review statistical analysis plans and related documents
  • Collaborate effectively with cross-functional stakeholders, including Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs
  • Work with in-house Documentation Specialists to produce high-quality final documents and ensure timely delivery
  • Mentor and develop junior medical writers, providing guidance and support as needed
  • Demonstrate advanced medical writing skills and maintain up-to-date knowledge of regulatory document requirements and guidelines
  • Work independently and as part of a team, managing multiple priorities and meeting challenging deadlines
  • Exhibit excellent interpersonal and presentation skills in all interactions
  • Maintain advanced proficiency in English for all written and verbal communications
WHAT YOU BRING
  • Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred)
  • 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas
  • Proven ability to autonomously write and review clinical regulatory documents (e.g., CTD Module II summaries, CSRs, Clinical Overviews, Investigator brochures, and other regulatory submissions)
  • Strong knowledge of regulatory document requirements and guidelines
  • Experience contributing scientifically and strategically to submission teams
  • Ability to plan data analyses and review statistical analysis plans for CSRs
  • Excellent collaboration skills with cross-functional stakeholders
  • Well-developed medical writing skills with attention to quality and deadlines
  • Ability to mentor and develop junior medical writers
  • Ability to work independently and as part of a team
  • Strong interpersonal and presentation skills
  • Advanced level of English proficiency
  • Ability to work under pressure and meet challenging deadlines
  • Remote work capability with availability in Eastern Standard Time (EST)