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Live In Regulatory Medical Writer Jobs (NOW HIRING)

... rooted in strong science and decades of regulatory experience - that will assist our clients in ... Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the ...

... in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Senior Medical Writer works under the direction of ...

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or ...

Analyst/Medical Writer

Boston, MA · On-site

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... In addition, you may have the chance to work on regulatory documents, lay summaries and policy ...

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

In addition to representing the Clinical Communications team as a content expert, the Principal ... legal/regulatory (MLR) review process requirements. * Medical Event Attendance: * Attend live ...

Our success has led to continued expansion both in the range of services we offer and our global presence. We are now looking for a talented and enthusiastic Senior Medical Writer. As a Senior ...

Medical Writer II

Portsmouth, NH · Hybrid

$115K - $125K/yr

... in the development and execution of clinical, scientific, and regulatory documents and ... We do that today by helping people with pelvic and gastrointestinal conditions live normal lives ...

... through regulatory challenges. The Senior Medical Writer will ensure high-quality content is ... In this role, the Senior Medical Writer has final sign-off authority and will review all ...

... through regulatory challenges. The Senior Medical Writer will ensure high-quality content is ... In this role, the Senior Medical Writer has final sign-off authority and will review all ...

Medical Writer

Cranbury, NJ · On-site

$55K - $60K/yr

As a Medical Writer with the Enterprise Content Team at MJH Life Sciences ® , you will play a vital role in developing educational content for healthcare professional audiences. This position offers ...

Accompany patient on errands or to medical appointments. * Light Housekeeping * Ensure clients ... Ability to read, write, speak, and understand English as needed for the job. * High School Diploma ...

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Live In Regulatory Medical Writer information

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How much do live in regulatory medical writer jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for live in regulatory medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Live In Regulatory Medical Writer vs Regulatory Medical Writer?

AspectLive In Regulatory Medical WriterRegulatory Medical Writer
CredentialsTypically requires a life sciences degree and medical writing certificationSame as Live In role, often with additional regulatory training
Work EnvironmentUsually based at a single location, living on-site or nearbyOffice-based or remote, depending on employer
Employer & IndustryPharmaceutical, biotech companies, or CROsPharmaceutical, biotech, or regulatory agencies
Search & Comparison IntentOften searched by those seeking on-site or live-in rolesMore general, including remote or office roles

Live In Regulatory Medical Writers focus on on-site, live-in roles within pharmaceutical or biotech companies, requiring specific certifications and a preference for on-location work. Regulatory Medical Writers may work remotely or in-office, with similar qualifications, but without the live-in component. The main difference lies in the work setting and living arrangements.

What cities are hiring for Live In Regulatory Medical Writer jobs? Cities with the most Live In Regulatory Medical Writer job openings:
What are the most commonly searched types of Regulatory Medical Writer jobs? The most popular types of Regulatory Medical Writer jobs are:
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMS

Aurora, CO • On-site

Full-time

Posted 25 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