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Senior Science 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 ... Write and edit clinical development documents, including but not limited to, clinical protocols ...

MMS

Senior Medical Writer (Remote)

Zionsville, IN · On-site

Our mission is to deliver high-quality service and technology solutions - rooted in strong science ... Write and edit clinical development documents, including but not limited to, clinical protocols ...

MMS

Senior Biostatistician - Remote (US)

Zionsville, IN · On-site

Senior Biostatistician: Responsibilities: * Create randomization and kit schedules independently ... Excellent scientific writing skills. * Strong resource for biostatistics; willing to guide others ...

INCOG

Tech Writer - Tech Services

Fishers, IN · On-site

... senior staff * Support creation of technical specifications, batch records, forms, and reports ... Associate's degree in English, Technical Writing, or scientific/technical discipline preferred * 0 ...

Pace

Formulation Associate Scientist

Indianapolis, IN · On-site

$23 - $25/hr

Join our mission to continuously move science forward; to innovate and advance all aspects of our ... This Associate Scientist will work under the guidance of senior scientists to execute formulation ...

Pacelabs

Formulation Associate Scientist

Indianapolis, IN · On-site

$23 - $25/hr

Join our mission to continuously move science forward; to innovate and advance all aspects of our ... This Associate Scientist will work under the guidance of senior scientists to execute formulation ...

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Senior Science Writer information

What is a senior science writer?

A Senior Science Writer is a professional who creates and edits scientific content for various audiences, including researchers, policymakers, and the general public. They work closely with scientists, subject matter experts, and communication teams to translate complex scientific information into clear, engaging, and accurate materials. Their work may include writing articles, reports, press releases, white papers, and grant proposals. They often have a background in science or journalism and must possess strong writing, research, and editing skills. Depending on the organization, they may also oversee junior writers, manage projects, and ensure consistency in scientific messaging.

What are typical daily responsibilities for a senior science writer?

A Senior Science Writer typically drafts and edits articles, research summaries, press releases, and technical documents for print or digital publication. They often interview scientists, attend research meetings, and translate complex data into accessible language for various audiences. Collaboration with editors, graphic designers, and subject matter experts is common to ensure accuracy and engaging presentation. Additionally, Senior Science Writers may mentor junior writers, contribute to editorial strategy, and help coordinate publication schedules, offering a dynamic and multifaceted work environment.

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

To thrive as a Senior Science Writer, you need exceptional writing and editing skills, advanced scientific literacy (often supported by a degree in a science discipline), and a proven track record in science communication. Familiarity with publishing platforms, reference management tools, and proficiency in editing or style guide systems (such as AMA or APA) is commonly expected. Outstanding soft skills include attention to detail, the ability to translate complex concepts for diverse audiences, project management, and collaborative teamwork. These capabilities ensure scientifically accurate, engaging content that meets both editorial standards and audience needs, while supporting collaboration with subject matter experts.

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Senior Science Writer jobs near you

Senior Medical Writer (Remote)

Zionsville, IN • On-site

MMS
Pharmaceutical and Medicine Manufacturing • 1 - 10 employees
Learn more about MMSexternal

Full-time

Posted 27 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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