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Entry Level Science Writing Jobs in Ohio (NOW HIRING)

Junior Java/C++ Developer

Cleveland, OH · On-site

$64K - $84K/yr

Excellent written and verbal communication skills Required Skills for Data Science/Machine Learning ... entry level position. The additional skills and project work with hands on experience building ...

Junior Backend Developer

Columbus, OH · On-site

$62K - $81K/yr

Excellent written and verbal communication skills For data Science/Machine learning REQUIRED SKILLS ... entry level position the additional skills and Project work with hands on experience building ...

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Entry Level Science Writing information

See Ohio salary details

$37.6K

$52.3K

$66.5K

How much do entry level science writing jobs pay per year?

As of Jul 2, 2026, the average yearly pay for entry level science writing in Ohio is $52,270.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,500.00 and $57,000.00 per year, depending on experience, location, and employer.

How to get a job in scientific writing?

To get a job in scientific writing, develop strong writing and research skills, often through a degree in science, journalism, or related fields. Build a portfolio of writing samples, gain experience through internships or freelance projects, and become familiar with scientific tools like reference management software. Networking with professionals and staying updated on industry trends can also improve job prospects.

Are science writers in demand?

Science writers are in steady demand as organizations seek clear communication of scientific information for diverse audiences. The role often requires strong writing skills, familiarity with scientific concepts, and the ability to use tools like content management systems; demand is expected to grow with increased emphasis on science literacy and public engagement.

How do I get a writing job with no experience?

Entry level science writing jobs often require strong writing skills, a basic understanding of scientific concepts, and the ability to communicate complex ideas clearly. Gaining experience through internships, volunteering, or creating a portfolio of writing samples can improve your chances; familiarity with tools like Microsoft Word or Google Docs is also helpful.

What is an Entry Level Science Writing job?

An Entry Level Science Writing job involves communicating scientific concepts, research findings, or technical information in a clear and accessible way for various audiences. Writers in this role may create articles, blog posts, reports, or educational materials for publications, organizations, or media outlets. Strong research skills, attention to detail, and the ability to translate complex topics into engaging content are essential. This role often serves as a stepping stone into more specialized science communication careers.

How much do science writers make?

Entry-level science writers typically earn between $40,000 and $60,000 annually, depending on experience, education, and location. Salaries can increase with specialization, portfolio quality, and additional skills such as editing or multimedia production.

What are the key skills and qualifications needed to thrive in the Entry Level Science Writing position, and why are they important?

Entry Level Science Writers should have a solid understanding of scientific concepts, strong research skills, and the ability to convey complex ideas in clear, accessible language, typically supported by a degree in science, journalism, or English. Familiarity with digital publishing tools, content management systems (CMS), and citation management software is often expected. Effective communication, attention to detail, and the ability to collaborate with subject matter experts are important soft skills. These competencies ensure accurate, engaging, and reliable science communication for diverse audiences.

What are typical daily tasks for an Entry Level Science Writer?

As an Entry Level Science Writer, your daily tasks will often include researching scientific topics, interviewing experts, and drafting articles, blogs, or reports based on your findings. You may be responsible for fact-checking, editing, and incorporating feedback from editors or senior scientists to ensure accuracy and clarity. Collaboration with graphic designers or multimedia teams to create engaging visuals can also be part of the role. This position offers a mix of independent work and teamwork, providing valuable exposure to both the communication and technical aspects of science writing.

What are the most commonly searched types of Science Writing jobs in Ohio? The most popular types of Science Writing jobs in Ohio are:
What are popular job titles related to Entry Level Science Writing jobs in Ohio? For Entry Level Science Writing jobs in Ohio, the most frequently searched job titles are:
What cities in Ohio are hiring for Entry Level Science Writing jobs? Cities in Ohio with the most Entry Level Science Writing job openings:
Infographic showing various Entry Level Science Writing job openings in Ohio as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $52,270 per year, or $25.1 per hour.
Entry-Level Study Start-Up Coordinator

Entry-Level Study Start-Up Coordinator

Medpace, Inc.

Cincinnati, OH

Other

Medical, PTO

Posted 4 days ago


Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

12th of 58 rated research


Job description

Job Summary

Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team. In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start-up process at Medpace. If you are seeking an exciting, entry-level position where you can build a foundation in the clinical research industry and develop/grow your career through our robust training program, then this is the opportunity for you.

Responsibilities
  • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
  • Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards); and
  • Maintain timelines for study start-up through internal team collaboration.

SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM

Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM Training Program embraces evidence based learning & development models to advance professional learning and employee performance. In the program, you will...

  • Complete independent learning modules, interactive exercises, and team workshops through the core curriculum;
  • Gain exposure to real-world tasks through a robust mentoring program; and
  • Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials.
Qualifications
  • Bachelor's degree is required (Life Sciences field preferred);
  • Some experience in an office setting is preferred;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office; and
  • Great attention to detail and excellent oral and written communication skills.

Travel: None

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards

  • Named a Top Workplace in 2024 by The Cincinnati Enquirer

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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