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Contract Medical Writer Jobs in Ohio (NOW HIRING)

Manage and supervise placement leaders, contract teams, and other site medical resources. * Provide ... Communicate effectively through written and verbal channels and conduct efficient meetings. * Build ...

Manage and supervise placement leaders, contract teams, and other site medical resources. * Provide ... Communicate effectively through written and verbal channels and conduct efficient meetings. * Build ...

Manage and supervise placement leaders, contract teams, and other site medical resources. * Provide ... Communicate effectively through written and verbal channels and conduct efficient meetings. * Build ...

Contract Attorney

Columbus, OH · Hybrid

$35 - $45/hr

... writing, particularly in the context of plaintiff-side litigation. Contract Attorney Responsibilities Conduct thorough legal research on issues related to personal injury, medical malpractice, and ...

Contract Attorney

Columbus, OH · Hybrid

$35 - $45/hr

... writing, particularly in the context of plaintiff-side litigation. Contract Attorney Responsibilities Conduct thorough legal research on issues related to personal injury, medical malpractice, and ...

Contract Supervisor

North Canton, OH · On-site

$90K - $100K/yr

Ability to read and interpret written information clearly and accurately. * Attention to detail and ... All traditional benefits offered, including 3 medical plan options and 2 dental plan options, as ...

Excellent verbal, written and interpersonal skills * Strong sense of urgency and self-initiative to ... Low-cost medical, dental, and vision insurance options. * Time Off: Personal leave, flexible ...

Excellent verbal, written and interpersonal skills * Strong sense of urgency and self-initiative to ... Low-cost medical, dental, and vision insurance options. * Time Off: Personal leave, flexible ...

Excellent verbal, written and interpersonal skills * Strong sense of urgency and self-initiative to ... Low-cost medical, dental, and vision insurance options. * Time Off: Personal leave, flexible ...

Excellent verbal, written and interpersonal skills * Strong sense of urgency and self-initiative to ... Low-cost medical, dental, and vision insurance options. * Time Off: Personal leave, flexible ...

$100K - $120K/yr

Demonstrated excellent written and verbal communication skill; ability to synthesize and translate ... Medical, dental and vision benefits * Paid Holidays * Company paid life insurance * 401(K) * Paid ...

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Showing results 1-20

Contract Medical Writer information

See Ohio salary details

$13

$36

$55

How much do contract medical writer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for contract medical 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 contract medical writer?

A Contract Medical Writer is a professional who creates scientific documents on a freelance or contract basis for pharmaceutical, biotech, or healthcare companies. They develop clinical study reports, regulatory submissions, manuscripts, and other medical content. Unlike full-time employees, contract medical writers work on a project-by-project basis, often remotely. They must have strong writing skills, scientific knowledge, and an understanding of medical regulations. This role offers flexibility but requires self-discipline and deadline management.

What are the key skills and qualifications needed to thrive as a contract medical writer?

To thrive as a Contract Medical Writer, you need a thorough understanding of scientific concepts, excellent writing skills, and often an advanced degree in life sciences or a related field. Familiarity with regulatory documentation formats (such as ICH, FDA, or EMA standards), medical journal requirements, and tools like Microsoft Office Suite or referencing software is vital. Strong organizational skills, attention to detail, and the ability to communicate complex information clearly are essential soft skills. These capabilities ensure accuracy, compliance, and the effective communication of scientific data to diverse audiences in the healthcare industry.

What types of projects can I expect to work on as a contract medical writer?

As a Contract Medical Writer, you may work on a variety of projects including clinical trial protocols, regulatory submissions, scientific manuscripts, patient education materials, and medical communications for conferences or publications. The work is typically project-based, with deadlines and deliverables defined by clients or pharmaceutical companies. You will often collaborate remotely with clinical researchers, regulatory teams, and subject matter experts to gather information and ensure accuracy. This diversity of projects keeps the role dynamic and allows for continuous learning in different therapeutic areas or document types.

What are the most commonly searched types of Medical Writer jobs in Ohio?

The most popular types of Medical Writer jobs in Ohio are:

What cities in Ohio are hiring for Contract Medical Writer jobs?

Cities in Ohio with the most Contract Medical Writer job openings:

Infographic showing various Contract Medical 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 16 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 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


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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