Freelance writer • thornton co
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 sub... Show more
Gana dinero grabando actividades de tu vida diaria.Buscamos personas para grabar actividades cotidianas desde una perspectiva en primera persona utilizando una aplicación móvil.Puedes grabar tareas... Show more
Join our team as a Spanish Interpreter (Contractor).We believe your skills and experience will be a valuable addition to our interpreting services.Role: Spanish Interpreter (Contractor) Work Type: ... Show more
This is an on-site position supporting mission-critical infrastructure at premier data center facilities.Rates vary based on experience level and project complexity.Emergency and after-hours work m... Show more
PRG is the world's leading technology provider within the entertainment and events industry.Our mission is to bring together the power of our people with our production and rental expertise to deli... Show more
Linguists are key players at TransPerfect.Your particular language skill and subject matter expertise will allow you to create and finalize the end product before it goes to the client.Under the gu... Show more
We are looking for a Service Writer to join our VW team! The right candidate will have automotive service advisor experience and a valid driver's license.The day-to-day duties of this role include ... Show more
Automotive Service Advisor / Writer.E 65th Ave, Denver, United States, 80249.This brand-new state-of-the-art facility is scheduled to open in Fall 2026 with interviews beginning this summer.As... Show more
SolRiver Capital is seeking a Renewable Energy Analyst.This position is for someone motivated to learn, with a head for finance, and passion for renewable energy.SolRiver is a leading renewable ene... Show more
Proposal Writer (Marketing Coordinator).Sandis is looking for a detail-oriented and collaborative Proposal Writer (Marketing Coordinator) to join our Marketing team remotely.Our ideal candidate wil... Show more
ProSidian Seeks a Technical Writer (On-site Scribe & AAR) | Dam Operator Safety Training: Fundamentals, Inspection, Monitoring & Field Practicum [DOI0015014] for Training on a Exempt 1099 Contract:... Show more
Acclaro combines cultural and language expertise with AI technology to help brands grow their global presence, connect with customers, and mean something to them.We are a trusted partner to some of... Show more
We're looking for a senior mechanical engineering expert to help build a benchmark of the hardest reasoning questions in the field — questions specifically designed to be difficult enough that toda... Show more
HOK is currently seeking an Architectural Specification Writer to join our team.This position can be filled in our Denver, Kansas City or St.The Architectural Specification Writer develops comprehe... Show more
We're looking for talented and motivated freelance Marketing Specialists to join our growing network.If you're creative, proactive, and passionate about helping businesses scale, we'd love to hear ... Show more
About Us Language Trainers is an international language training company working with freelance teachers of 99+ languages in hundreds of cities worldwide.Founded in 2004, our motto is Any Language,... Show more
Experienced Workers' Compensation Professional.We are seeking an experienced workers' compensation professional to work with clients to control costs and exposure and help injured workers get back ... Show more
Provides subject matter expertise for the change management necessitated by the OIT CTO organizational transformation initiative:.Coordinates with OIT and the CTO Transformation Program Manager and... Show more
Role Overview** Mercor is partnering with a leading AI research organization to engage experienced UI/UX and product designers for a project focused on evaluating how well AI systems perform real-w... Show more
The average salary range is between $ 41,600 and $ 117,836 year , with the average salary hovering around $ 57,157 year .
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 Powered by JazzHR
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