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Scientific Medical Writer Jobs in Indiana (NOW HIRING)

MMS

Senior Medical Writer (Remote)

Zionsville, IN · On-site

Our mission is to deliver high-quality service and technology solutions - rooted in strong science ... Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the ...

Veristat

Bachelor's degree required; science-related field preferred. Minimum of 7 years of medical writing ... experience in a contract research organization or pharmaceutical/biotechnology research setting.

CYNET SYSTEMS

Medical Writer I_CO

Indianapolis, IN · On-site

$42/hr

A Bachelor's degree in a life science, engineering, or technical discipline, or in journalism ... At least 3+ years of demonstrated professional technical writing experience is necessary.

GlaxoSmithKline

SERM Scientific Director

Warsaw, IN · On-site

Immunology Provides in-depth medical/scientific expertise in the safety evaluation and risk ... Authors/participates in written standard updates (e.g., SOPs) to ensure policies and regulations ...

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Scientific Medical Writer information

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How much do scientific medical writer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for scientific medical writer in Indiana is $44.03, according to ZipRecruiter salary data. Most workers in this role earn between $32.02 and $53.32 per hour, depending on experience, location, and employer.

What is a scientific medical writer?

A Scientific Medical Writer creates clear, accurate, and well-structured documents related to medical and scientific information. They translate complex research data into formats such as journal articles, regulatory documents, clinical study reports, and educational materials. These professionals work closely with researchers, healthcare professionals, and regulatory teams to ensure scientific accuracy and compliance with industry guidelines. Strong writing skills, scientific knowledge, and attention to detail are essential for success in this role.

What are the typical work settings and team dynamics for a scientific medical writer?

Scientific Medical Writers commonly work in pharmaceutical companies, medical communications agencies, academic institutions, or as independent consultants, often collaborating within cross-functional teams that include researchers, clinicians, regulatory experts, and marketing professionals. Daily responsibilities involve drafting, reviewing, and revising scientific manuscripts, clinical study reports, and regulatory documents, often under tight deadlines. While some positions are office-based, there are increasing opportunities for remote or hybrid work environments. Collaboration, adaptability, and regular communication with subject matter experts are central to success in this field, as writers must ensure both scientific accuracy and audience-appropriate messaging.

What are the key skills and qualifications needed to thrive in a scientific medical writer position, and why are they important?

To thrive as a Scientific Medical Writer, you need advanced scientific knowledge, exceptional writing and editing abilities, and typically a degree in life sciences or a related field. Familiarity with reference management software, publication guidelines (such as GPP or ICMJE), and medical literature databases is highly beneficial. Attention to detail, strong project management, and clear communication skills help differentiate top performers in this role. These competencies ensure the accurate, compliant, and effective communication of complex scientific information to a variety of audiences.

How to become a scientific medical writer?

To become a scientific medical writer, typically a bachelor's degree in a life science or related field is required, often complemented by advanced degrees such as a master's or PhD. Developing strong writing skills, understanding scientific research, and gaining experience through internships or entry-level positions are important steps; familiarity with medical terminology and tools like reference management software can also be beneficial.

Is there a demand for scientific medical writers?

There is strong demand for scientific medical writers due to the growth of the healthcare and pharmaceutical industries, as well as increased regulatory requirements for clinical documentation and medical communications. Professionals with expertise in scientific writing, knowledge of medical terminology, and familiarity with industry tools are sought after in both pharmaceutical companies and contract research organizations.

What are popular job titles related to Scientific Medical Writer jobs in Indiana?

For Scientific Medical Writer jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Scientific Medical Writer jobs in Indiana look for?

The top searched job categories for Scientific Medical Writer jobs in Indiana are:

What cities in Indiana are hiring for Scientific Medical Writer jobs?

Cities in Indiana with the most Scientific Medical Writer job openings:

Scientific Medical Writer jobs near you
Infographic showing various Scientific Medical Writer job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, and 5% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $91,574 per year, or $44 per hour.

Senior Medical Writer (Remote)

MMS

Zionsville, IN • On-site

Full-time

Posted 23 days ago

Key responsibilities

  • Critically evaluate, analyze, and interpret medical literature to select primary resource materials for study design and scientific rigor.

  • Write and edit clinical development documents such as protocols, investigator's brochures, clinical study reports, and regulatory submission materials.

  • Manage timelines and workflow of writing assignments, coordinate with clients and project team members, and take ownership of specific assignments.

Job description

About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
  • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • Mentor medical writers and other members of the project team who are involved in the writing process
Requirements
  • At least 3 years of previous experience in the pharmaceutical industry
  • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
  • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • Exceptional writing skills are a must
  • Excellent organizational skills and the ability to multi-task are essential prerequisites
  • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
  • Experience being a project lead, or managing a project team
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

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M. M. S. logo

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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