Senior Medical Writer (Remote - Mexico)

MMS Holdings Inc; México; Remote; MXN 480,000 - 720,000; Full time

Job summary

MMS Holdings Inc, a data-focused CRO, seeks a Medical Writer to critically evaluate literature and craft regulatory documents including protocols, study reports, and safety summaries. You will lead writing projects, mentor junior writers, and coordinate with clients to meet aggressive timelines in a remote Mexico setting.

The ideal candidate has 3+ years in pharma regulatory writing, advanced degree, and strong skills in MS Word/Excel/PowerPoint.

Qualifications

• Minimum 3 years in pharmaceutical industry.
• 3–5 years of regulatory writing experience.
• Bachelor's/Master's/Ph.D. in scientific/medical field.
• Lead author on substantial clinical study protocols.
• Experience with regulatory submissions is a plus.

Responsibilities

• Evaluate and interpret medical literature to select primary materials for study design and regulatory documents.
• Write and edit clinical development documents (protocols, brochures, study reports, consent forms, summaries).
• Manage writing assignments and maintain timelines and workflow.
• Mentor writers and project team members on writing processes.
• Lead and coordinate with client teams to ensure timely delivery.

Skills

Regulatory writing

Project leadership

Excellent writing

Time management

Education

Bachelor's/Master's/PhD in scientific/medical field

Tools

MS Word

MS Excel

PowerPoint

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMS is aaward-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

We are looking for a full-time employee, remotelybased within any location in Mexico.

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.