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Senior Medical Editor Jobs in Indiana (NOW HIRING)

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Sr. Medical Writer ICON is a global healthcare intelligence and clinical research organisation ... Leading the preparation, review, and editing of clinical study documents, including clinical study ...

pepperconstruction

Marketing Coordinator

Indianapolis, IN · On-site

$40K - $55K/yr

More tenured candidates could be considered for a Senior Proposal/Marketing Coordinator title ... Bonus points for experience with video editing and photography (we love a good camera moment). * A ...

pepperconstruction

Marketing Coordinator

Indianapolis, IN

$40K - $55K/yr

More tenured candidates could be considered for a Senior Proposal/Marketing Coordinator title ... Bonus points for experience with video editing and photography (we love a good camera moment). * A ...

DPDHL

Administrative Assistant I

Jeffersonville, IN · On-site

$51K - $55K/yr

Provide advanced administrative support for senior management as well as courteous, responsive and ... Our excellent benefits packages includes: - Affordable medical, dental, and vision coverage ...

DPDHL

Administrative Assistant I

Jeffersonville, IN · On-site

$51K - $55K/yr

Provide advanced administrative support for senior management as well as courteous, responsive and ... Our excellent benefits packages includes: - Affordable medical, dental, and vision coverage ...

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All JobsMedical Editor JobsSenior Medical Editor JobsSenior Medical Editor Jobs in Indiana

Senior Medical Editor information

See Indiana salary details

$35.2K

$79.1K

$114.7K

How much do senior medical editor jobs pay per year?

As of Aug 21, 2026, the average yearly pay for senior medical editor in Indiana is $79,085.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,900.00 and $99,400.00 per year, depending on experience, location, and employer.

What does a senior medical editor do?

A Senior Medical Editor reviews, edits, and ensures the accuracy and clarity of medical and scientific documents, such as manuscripts, regulatory submissions, and educational materials. They work closely with writers, researchers, and project managers to maintain consistency with style guidelines and regulatory requirements. Additionally, Senior Medical Editors may mentor junior editors, oversee quality control processes, and ensure that all materials are scientifically sound and suitable for the intended audience.

How does a senior medical editor typically collaborate with medical writers and subject matter experts during the content development process?

Senior Medical Editors play a key role in ensuring the accuracy, clarity, and compliance of medical content. They work closely with medical writers to review and refine manuscripts, providing detailed feedback on scientific accuracy, consistency, and adherence to style guidelines. Additionally, they regularly interact with subject matter experts to verify technical details and ensure that complex information is communicated effectively to the intended audience. Strong collaboration and communication skills are essential, as Senior Medical Editors often coordinate between cross-functional teams to meet project deadlines and maintain high editorial standards.

What are the key skills and qualifications needed to thrive as a senior medical editor, and why are they important?

To thrive as a Senior Medical Editor, you need advanced expertise in medical writing, a solid understanding of scientific research, and typically a degree in life sciences or a related field. Familiarity with style guides (such as AMA or ICMJE), reference management software, and document review systems is important. Outstanding attention to detail, strong communication, and the ability to manage multiple projects set top performers apart. These skills ensure the accuracy, clarity, and compliance of medical content, which is crucial for regulatory submissions and effective knowledge dissemination.

What is the difference between Senior Medical Editor vs Medical Writer?

AspectSenior Medical EditorMedical Writer
CredentialsTypically requires advanced degrees (MD, PhD, or PharmD) and editing certificationsUsually holds degrees in life sciences or related fields; writing certifications are common but not mandatory
Work EnvironmentEditorial teams within pharmaceutical, biotech, or healthcare companies; publishing agenciesContent creation in pharmaceutical, medical communications, or healthcare marketing firms
Employer & Industry UsageUsed in medical publishing, regulatory agencies, and pharma companies for content reviewCommon in medical writing agencies, pharma marketing, and clinical documentation

The main difference is that Senior Medical Editors focus on reviewing and refining medical content for accuracy and clarity, often overseeing editing teams, while Medical Writers primarily create original medical content. Both roles require strong medical knowledge, but Senior Medical Editors emphasize editing and quality control.

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

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

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

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

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

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

Senior Medical Editor jobs near you
Infographic showing various Senior Medical Editor job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $79,085 per year, or $38 per hour.

Sr Medical Writer

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On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 20 days ago

Job description

Sr. Medical Writer

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will take ownership of medical writing deliverables, applying your expertise to complex challenges.
Key responsibilities include:

  • Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity
  • Collaborating closely with cross-functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarize scientific findings
  • Participating in the planning and execution of clinical development programs, providing strategic input and scientific expertise to support the design, conduct, and interpretation of clinical studies and research initiatives.
  • Contributing to the development of publication plans, abstracts, posters, and manuscripts for submission to peer-reviewed journals and presentation at scientific conferences
  • Mentoring and coaching junior medical writers, providing guidance on best practices, writing techniques, and scientific principles, and fostering a culture of excellence, collaboration, and continuous learning within the medical writing team.

Your Profile:

You will have a strong foundation in medical writing, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Proficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skills
  • Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process.
  • Demonstrated ability to work effectively in a fast-paced, deadline-driven environment, managing multiple projects simultaneously and prioritizing tasks based on project timelines and deliverables.
  • Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams, build relationships with key stakeholders, and influence decision-making processes.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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