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Medical Science Writer Jobs in Ohio (NOW HIRING)

The Principal Medical Writer, in partnership with a project lead, leverages strategic and ... Is recognized as a strong scientific contributor and collaborator on cross-functional teams and ...

New

Technical Writer

Beavercreek, OH · On-site

$100 - $125/hr

KBR's work is at the forefront of engineering, logistics, operations, science, program management ... KBR Benefits * 401K plan with company match * medical * dental * vision * life insurance * AD&D ...

$125 - $150/hr

Extensive experience in (scientific) communications at an agency and/or in the pharmaceutical industry * Proven experience in medical writing and medical education--experience in medical consulting ...

Liaises with clients or developers to gather information; and Organizes, synthesizes medical and ... IT Life Sciences Allied Healthcare CRO DIRECT # - (650)-399-0891 Gold Seal JCAHO Certified for ...

Showing results 41-60

Medical Science Writer information

See Ohio salary details

$13

$36

$55

How much do medical science writer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for medical science writer in Ohio is $36.73, according to ZipRecruiter salary data. Most workers in this role earn between $24.90 and $46.39 per hour, depending on experience, location, and employer.

What is a medical science writer?

Medical Science Writers are professionals who create scientific documents related to medicine, healthcare, and clinical research. They translate complex scientific and clinical information into clear, accurate, and accessible content for various audiences, such as healthcare professionals, regulatory agencies, or the general public. Their work includes writing research articles, regulatory documents, educational materials, and marketing content. Medical Science Writers often work for pharmaceutical companies, medical communication agencies, academic institutions, or as freelancers.

How does a medical science writer typically collaborate with subject matter experts and project teams?

Medical Science Writers frequently work with physicians, researchers, and regulatory professionals to create accurate and clear scientific documents. Collaboration often involves conducting interviews, reviewing complex data, and ensuring all materials meet industry and regulatory standards. Writers may participate in team meetings, provide content drafts for review, and incorporate feedback from multiple stakeholders. This collaborative environment helps ensure the final documents are scientifically rigorous and tailored to the intended audience, whether that be regulatory agencies, healthcare professionals, or the public.

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

To thrive as a Medical Science Writer, you need a solid background in life sciences or medicine (often with an advanced degree), strong writing skills, and the ability to interpret complex scientific data. Familiarity with referencing software, medical databases, and style guides such as AMA or ICMJE is typically required. Attention to detail, critical thinking, and the ability to communicate clearly with both scientific and non-scientific audiences are essential soft skills. These competencies ensure accurate, credible, and accessible medical content that supports both regulatory compliance and effective information dissemination.

Do medical science writers make good money?

Medical science writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced writers with specialized knowledge can earn over $100,000 per year. Strong writing skills, scientific background, and familiarity with industry tools can enhance earning potential.

How to become a medical science writer?

To become a medical science writer, typically a bachelor's degree in life sciences, health sciences, or a related field is required, often complemented by strong writing skills and knowledge of scientific concepts. Many professionals pursue advanced degrees or certifications in science communication or medical writing, and gaining experience through internships or freelance projects can be beneficial. Familiarity with medical terminology, research methods, and tools like reference management software is also important.

Is there a demand for medical science writers?

Medical science writers are in high demand due to the growing need for clear communication of complex scientific and medical information. They are employed in pharmaceutical companies, healthcare organizations, and research institutions, often requiring strong writing skills and knowledge of scientific tools and regulations. The field is expected to grow as medical research and healthcare industries expand globally.

What are popular job titles related to Medical Science Writer jobs in Ohio?

For Medical Science Writer jobs in Ohio, the most frequently searched job titles are:

Infographic showing various Medical Science Writer job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 14% Part Time, 1% Temporary, and 7% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $76,401 per year, or $36.7 per hour.

Medical Writer - PhD - Hematology/Oncology - Cincinnati

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

16th of 75 rated research


Job description

Job Summary

Medpace is currently seeking candidates with a PhD in Life Sciences with a focus in Hematology and/or Oncology research for a full-time, office-based Medical Writer position. The Medical Writer will lead development of various high-quality documents critical to the development of safe and effective medical therapeutics. This is a unique opportunity that includes comprehensive training and application of the candidate's analytical skills and academic knowledge. The position includes independent work and cross-functional collaboration. If you want a rewarding position that allows you to be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Responsibilities

Write, edit, and maintain high-quality, complex clinical and regulatory documents, including, but not limited to, clinical study reports, protocols, Investigator's brochures, and IND and NDA modules; Coordinate and conduct quality control reviews; Effectively communicate and collaborate with Sponsors and Medpace subject matter experts; Manage multiple projects and tasks simultaneously while also meeting deadlines; and Maintain an understanding of and compliance with company processes, and industry guidelines and regulations.

Qualifications

PhD in Life Sciences with a focus in Hematology and/or Oncology research (clinical or nonclinical); Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience; Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992