Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Statistical, analysis background with experience in SQL databases, experience in medical writing. Strong inter-personal skills both written and verbal required, effective verbal and written ...
Statistical, analysis background with experience in SQL databases, experience in medical writing. Strong inter-personal skills both written and verbal required, effective verbal and written ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. Preferred Qualifications * Experience in pharmaceutical, biotechnology ...
Medical Writing information
See Ohio salary details
$10.97 - $16.79
0% of jobs
$16.79 - $22.60
8% of jobs
$22.60 - $28.42
12% of jobs
$31.18 is the 25th percentile. Wages below this are outliers.
$28.42 - $34.24
11% of jobs
$34.24 - $40.06
11% of jobs
The median wage is $42.66 / hr.
$40.06 - $45.87
20% of jobs
$51.38 is the 75th percentile. Wages above this are outliers.
$45.87 - $51.69
15% of jobs
$51.69 - $57.51
13% of jobs
$57.51 - $63.32
7% of jobs
$63.32 - $69.14
2% of jobs
$69.14 - $74.96
2% of jobs
$10
$43
$74
How much do medical writing jobs pay per hour?
As of Aug 22, 2026, the average hourly pay for medical writing in Ohio is $43.99, according to ZipRecruiter salary data. Most workers in this role earn between $31.97 and $53.27 per hour, depending on experience, location, and employer.
What is medical writing?
Medical writing is the process of creating scientific documents by specialized writers in the healthcare, pharmaceutical, or biotechnology industries. These documents can include clinical trial reports, regulatory submissions, research manuscripts, patient education materials, and more. Medical writers must accurately present complex medical information in a clear, concise, and compliant manner, often working closely with researchers, doctors, and regulatory professionals. The role requires a strong understanding of medical terminology, scientific research, and regulatory guidelines.
What are medical writing jobs?
Medical writing jobs work in health care and science communities to compose documents and articles. Those who have medical writing jobs may draft many different kinds of papers, such as educational or promotional literature, medical abstracts for textbooks, or research documents. Other medical writing jobs include ghost-writing for prominent scientists or physicians, journalistic writing for scientific magazines, or creating content for marketing materials. Regardless of what field you are in, to obtain medical writing jobs, you must be able to decipher and interpret complicated information and write in a manner that your audience understands. For example, you may use medical jargon in scientific journals, but medical writers typically use simpler language when writing for the general public.
What are the key skills and qualifications needed to thrive as a medical writer, and why are they important?
To thrive as a Medical Writer, you need strong scientific knowledge, excellent written communication skills, and typically a background in life sciences or healthcare. Familiarity with referencing software, regulatory guidelines, and document management systems is often required. Attention to detail, adaptability, and the ability to explain complex concepts clearly are valuable soft skills in this role. These abilities ensure the accurate and effective communication of medical information for regulatory, clinical, or educational purposes.
How does a medical writer typically collaborate with subject matter experts and regulatory teams during a project?
Medical writers regularly interact with subject matter experts (such as clinicians and researchers) to ensure scientific accuracy and clarity in documents like clinical study reports, publications, or regulatory submissions. They also work closely with regulatory teams to align content with current guidelines and submission requirements. This collaboration often involves attending meetings, managing document reviews, and incorporating diverse feedback to produce high-quality, compliant deliverables. Effective communication and project management skills are essential to coordinate these multi-disciplinary efforts and meet strict deadlines.
What is the difference between Medical Writing vs Medical Editing?
| Aspect | Medical Writing | Medical Editing |
|---|---|---|
| Required Credentials | Typically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writing | Requires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields |
| Work Environment | Often works independently or in teams, creating clinical documents, regulatory submissions, and educational materials | Usually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency |
| Employer & Industry Usage | Used in pharmaceutical, biotech, healthcare, and medical device industries | Common in publishing, healthcare communications, and regulatory agencies |
Medical Writing involves creating original medical content such as clinical study reports, regulatory documents, and educational materials. Medical Editing focuses on reviewing and refining these documents to ensure clarity, accuracy, and compliance. Both roles require strong medical knowledge, but Medical Writers produce content, while Medical Editors improve existing content.
Do medical writers make good money?
Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals or those with specialized skills can earn over $100,000 per year. Many medical writers also have opportunities for freelance work or consulting, which can impact income levels.
How do I become a medical writer?
To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often complemented by advanced degrees or certifications in medical writing or regulatory writing. Developing strong writing skills, understanding scientific and medical terminology, and gaining experience through internships or entry-level positions are important steps; familiarity with tools like Microsoft Word and reference management software can also be beneficial.
Is there a demand for medical writers?
Yes, there is a strong demand for medical writers due to the growth of the healthcare and pharmaceutical industries, regulatory requirements, and the need for clear scientific communication. Medical writers often work in pharmaceutical companies, medical communications agencies, or as freelancers, and proficiency in scientific terminology and regulatory guidelines enhances job prospects.
What does the medical writer do?
A medical writer creates clear, accurate, and scientifically supported documents such as research articles, regulatory submissions, clinical study reports, and patient education materials. They interpret complex medical data for diverse audiences and often work with subject matter experts, adhering to industry guidelines and using tools like reference management software. Strong writing skills and knowledge of medical terminology are essential for this role.
More about Medical Writing jobs
What are the most commonly searched types of Medical Writing jobs in Ohio?
The most popular types of Medical Writing jobs in Ohio are:
What are popular job titles related to Medical Writing jobs in Ohio?
For Medical Writing jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Medical Writing jobs in Ohio look for?
The top searched job categories for Medical Writing jobs in Ohio are:
What cities in Ohio are hiring for Medical Writing jobs?
Cities in Ohio with the most Medical Writing job openings:
Full-time
This job post has expired 1 day ago. Applications are no longer accepted.
Job description
We are seeking an experienced Principal Statistical Programmer to lead statistical programming activities for clinical development programs. The ideal candidate will have strong expertise in SAS programming, CDISC standards, ADaM datasets, TLF development, regulatory submissions, and clinical trial data analysis. This role will provide technical leadership, mentor statistical programmers, and collaborate with cross-functional clinical teams.
Required Skills & Experience- Experience leading a team of statistical programmers supporting clinical development programs.
- Strong proficiency in SAS programming for developing and validating:
- ADaM datasets
- Tables, Listings, and Figures (TLFs)
- Statistical analyses
- Good knowledge of R programming and other statistical programming languages preferred.
- Strong understanding of SAS programming concepts and the clinical study lifecycle.
- In-depth knowledge of CDISC standards (SDTM/ADaM) and regulatory requirements.
- Experience supporting regulatory filings and submission documentation.
- Experience working in therapeutic areas such as Oncology, Immunology, Neuroscience, or similar domains.
- Strong communication and collaboration skills with cross-functional teams.
- Ability to estimate project programming efforts and manage competing priorities.
- Lead statistical programming activities for assigned compounds, indications, or therapeutic areas.
- Manage and mentor statistical programmers, analysts, and senior analysts.
- Plan resources, track deliverables, and ensure timely completion of programming activities.
- Develop and oversee SAS programs for ADaM dataset creation following CDISC standards.
- Develop and review SAS programs for Tables, Listings, and Figures (TLFs).
- Ensure consistency and quality of ADaM datasets across individual studies and integrated analyses.
- Support regulatory submissions by preparing documentation such as reviewer guides and data definition documents.
- Develop standard SAS macros, programming standards, and operating procedures.
- Ensure compliance with quality processes and clinical programming best practices.
- Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams.
- Experience in pharmaceutical, biotechnology, or clinical research environments.
- Strong knowledge of clinical trial programming and regulatory submission processes.
- Excellent leadership, problem-solving, and organizational skills.
- Ability to work effectively in a dynamic, deadline-driven environment.