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Senior Medical Writer Jobs in Indiana (NOW HIRING)

MMS

Senior Medical Writer (Remote)

Zionsville, IN · On-site

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 ...

SMC

Senior Assembler

Noblesville, IN · On-site

Senior Assembler The purpose of the Senior Assembler position is to accurately perform tasks ... Must be able to read/write/speak and understand English. Must be able to effectively communicate.

SMC

Senior Assembler

Noblesville, IN · On-site

Senior Assembler The purpose of the Senior Assembler position is to accurately perform tasks ... Must be able to read/write/speak and understand English. Must be able to effectively communicate.

Labcorp

Senior Medical Technologist

Indianapolis, IN · On-site

Labcorp is seeking a Senior Medical Technologist to join our Immunolgy team in Indianapolis, IN ... Initiates revisions to SOPs or writes new SOPs to reflect current processes that ensure compliance.

CAPS & Maple City

Medical Assistant - Senior

Goshen, IN

$21.29 - $25.26/hr

Description Job Title: Medical Assistant - Senior Reports to: MA Coordinator Supervisory ... Ability to run/write routine reports and documentation * Ability to speak effectively to the public ...

CAPS & Maple City

Medical Assistant - Senior

Goshen, IN · On-site

$21.29 - $25.26/hr

Medical Assistant - Senior Reports to: MA Coordinator Supervisory Responsibilities: Medical site ... Ability to run/write routine reports and documentation * Ability to speak effectively to the public ...

Relativity

Senior Billing Specialist

Indianapolis, IN · On-site

$60K - $90K/yr

Effective communicator with excellent verbal and written communication skillswithability topositivelycollaborate with cross-functional teams and senior leadership * Prior experience in a high-growth ...

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Senior Medical Writer information

See Indiana salary details

$33.3K

$130.6K

$235.5K

How much do senior medical writer jobs pay per year?

As of Aug 30, 2026, the average yearly pay for senior medical writer in Indiana is $130,637.00, according to ZipRecruiter salary data. Most workers in this role earn between $99,000.00 and $158,000.00 per year, depending on experience, location, and employer.

What is a senior medical writer?

A Senior Medical Writer is responsible for creating clear, accurate, and compliant medical documents, including regulatory submissions, clinical study reports, and scientific publications. They work closely with cross-functional teams, such as medical affairs, regulatory affairs, and clinical teams, to ensure high-quality content. Senior Medical Writers also review and edit documents for consistency, clarity, and adherence to industry guidelines. Often, they mentor junior writers and contribute to process improvements within the medical writing team.

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

To thrive as a Senior Medical Writer, you need advanced writing and editing skills, a thorough understanding of scientific and medical concepts, and typically a degree in a life science or related field. Familiarity with referencing tools (like EndNote), document management systems, and compliance with regulatory guidelines (such as ICH or FDA standards) is often required. Strong attention to detail, project management abilities, and the capacity to communicate complex ideas clearly are important soft skills for this position. These competencies ensure accurate, high-quality medical content that meets industry standards and supports effective communication among healthcare professionals and stakeholders.

What are some common challenges faced by senior medical writers, and how can they be addressed?

Senior Medical Writers often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring adherence to strict regulatory requirements. To navigate these challenges, it's essential to have strong organizational skills, effective communication with project teams, and a solid grasp of industry guidelines. Many Senior Medical Writers find that staying current with new regulations, participating in ongoing professional development, and leveraging collaborative tools help streamline the workflow. By proactively addressing these challenges, writers can maintain accuracy and efficiency while contributing valuable expertise to cross-functional teams.

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

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

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

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

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

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

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

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

What are popular job titles related to Senior Medical Writer jobs in IN?

For Senior Medical Writer jobs in IN, the most frequently searched job titles are:

Senior Medical Writer jobs near you
Infographic showing various Senior 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 $130,637 per year, or $62.8 per hour.

Senior Medical Writer (Remote)

MMS

Zionsville, IN • On-site

Full-time

Posted 17 days ago

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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