Science 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
Kansas City, MO; Denver, CO; Chicago, IL; New York, NY; Remote.MissionOne Media is a brand within BarkleyOKRP that combines full-funnel media planning and buying services, CRM, data, analytics, ret... Show more
This is an exceptional, hands-on, player/coach opportunity to establish, shape, and lead our Data Science capability in the United States.As the Data Science Team Leader, you will be a critica... Show more
Director Of Sales And Marketing Life Science.Are you looking for an opportunity to make a difference? At Mesa Labs we're passionate about protecting the vulnerable by enabling scientific breakthro... Show more
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Focuses on growing presence and market share in identified markets aligned with HKS's practice and geographic areas of strategic growth.Leads pursuit and development activity of new client relation... Show more
Was previously named "Law Firm of the Year" in Patent Law.Collaborative work culture, with a realistic chance to make Partner.Recognized by BTI Consulting for Strong Client Relationships.Ideal cand... Show more
Empower students in a mission-driven K–12 charter community!.Join a team committed to excellence and equity!.Collaborate with passionate educators and families!.Thrive in a supportive, studen... Show more
About Us:Global Village Academy is an innovative charter school.Students learn core content through language immersion in their choice of French, Spanish or Mandarin Chinese.GVA is truly a "global ... Show more
At MERGE, we are Built Different.We are a marketing and technology agency purpose-built for the intersection of health and wellnesswhere human impact matters most.By weaving storytelling through te... Show more
Senior Product Manager, AI & Data Science Products.The Senior Product Manager, AI & Data Science Products owns Crunchbase's customer-facing AI data layer: proprietary data and intelligence generate... Show more
MissionOne Media is a brand within BarkleyOKRP that combines full-funnel media planning and buying services, CRM, data, analytics, retail media, SEO, and digital experiences.Our tech stack is power... Show more
FRCC Business and Computing Technology.Boulder County Campus, Larimer Campus, Westminster Campus, Online Learning.Longmont, CO; Fort Collins, CO; Westminster, CO; Remote (Colorado).Please see Addit... Show more
This is an exceptional, hands-on, player/coach opportunity to establish, shape, and lead our Data .Science capability in the United States.As the Data Science Team Leader, you will be a critical pa... Show more
Perkins&Will Denver Studio is seeking accomplished Project Manager with 8-10+ years of experience in leading projects, who are adept at steering the full spectrum of the design processfrom concept... Show more
THIS POSTION IS FOR A MONDAY EARLY AFTERNOON POSITION WITH ROOM TO GROW FOR MORE SHIFTS.Get paid to have fun hanging out with kids,.Lead Art Instructors are required to instruct art and science cla... Show more
Application deadline: Sep 27, 2026.Do you want to solve business challenges through innovative technology? Do you enjoy working on cutting-edge, scalable services technology in a team environment? ... Show more
At Johnson & Johnson,we believe health is everything.Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are ... Show more
Develop and conduct program and policy analyses to identify and understand the needs and preferences of HHS health and human services programs and the populations they serve.Utilize appropriate mar... Show more
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
