Senior Medical Writer (Remote)

MMS; San Antonio (TX); Remote; USD 80,000 - 100,000; Full time

Job summary

A leading CRO in San Antonio is seeking a Senior Medical Writer to produce clinical development documents. The ideal candidate will have extensive regulatory writing experience and a strong background in clinical study protocols. This role requires excellent writing and organizational skills, along with proficiency in MS Office tools. Join a dynamic team focused on delivering high-quality submissions to meet regulatory standards.

Qualifications

• At least 3-5 years of regulatory writing and clinical medical writing experience.
• Substantial clinical study protocol experience, as lead author, required.

Responsibilities

• Write and edit clinical development documents including protocols and reports.
• Maintain timelines and workflow of writing assignments.
• Mentor medical writers and project team members.

Skills

Writing

Organizational Skills

Communication

Education

Bachelor's, Master's, or Ph.D. in scientific, medical, clinical discipline

Tools

MS Word

Excel

PowerPoint

Job description

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.

Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.

With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma’sinternational awards programs for the last three consecutive years.

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 Substantial clinical study protocol experience, as lead author, required Experience leading and managing teams while authoring regulatory documents with aggressive timelines Not required, but experience with orphan drug designations and PSP / PIPs a plus Powered by JazzHR

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Senior Medical Writer • San Antonio, TX, US