Curriculum writer • lakewood 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
Medical Writer / Clinical Document Author.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance,... Show more
Orders, replenishes and merchandises grocery products and participate in WFM program for purchasing and promotions.Monitors inventory control and replenishes product based upon WFM ordering standar... Show more
The Odyssey School of Denver is a diverse, K-8 Expeditionary Learning (EL) charter school.We believe in teaching students how to learn by focusing on academic achievement, critical thinking, and so... Show more
We're looking for a senior aerodynamics expert to help build a benchmark of the hardest reasoning questions in the field — questions specifically designed to be difficult enough that today's most c... Show more
Proposal Writer, Sr | Lockheed Martin.The Proposal Writer, Sr will apply proven writing and communications skills to support the development of compelling narratives through drafting, messaging, an... Show more
Medical Writer / Clinical Document Author.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance,... Show more
As an Education Coach at Primrose School of Denver Central Park, you will play a critical role in driving educational excellence.You will mentor and coach teachers, support classroom quality, and c... Show more
The Senior Product Owner: Integrations is responsible for driving product integration success by maximizing the value delivered by their teams, ensuring alignment with customer and stakeholder need... Show more
Savvas Learning Company is a global education company that produces award-winning learning solutions that empower educators and engage students with the highest quality content.Recognized as an ind... Show more
Facilities & Engineering Investigation Writer.The Facilities & Engineering Investigation Writer reports to the Vice President, Facilities and Engineering and is responsible for leading critical inv... 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
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
Join Our Pursuit Strategy & Proposal Team.Our "we-care" culture is more than just a motto; it's a promise.From day one, we prioritize your growth, well-being, and success.You can count on us to sup... Show more
Medical Writer / Clinical Document Author.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance,... Show more
Campus Director Of Curriculum And Instruction (DCI).Grade Level: High School (9th - 12th); Middle School (6th - 8th).Salary: $77,500-$92,500 based on years of aligned experience, up to 10 years.We ... 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
As an Education Coach at Primrose School of Denver Central Park, you will play a critical role in driving educational excellence.You will mentor and coach teachers, support classroom quality, and c... Show more
University of Colorado Anschutz Medical Campus Department: Office of Medical Education Job Title: Clinical Pillar Team Lead Position #: 00786015 Requisition #:40348 Job Summary: The Clinical Pilla... 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
The average salary range is between $ 50,583 and $ 121,875 year , with the average salary hovering around $ 69,000 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
