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MMS
Paradise Valley
Job Description 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
Job Source: MMSCardinal Health
Phoenix, AZ, United States
**_What Medical Writing contributes to Cardinal Health_** The Medical Writing Project Manager is a member of the Medical Affairs team, within in Global Medical Products, and is responsible for the planning, development, writing and reviewing Post Market Surveillance Plans and Clinical Evaluation Reports for the medical devices. The Project Manage
Job Source: Cardinal HealthCardinal Health
Phoenix
**_What Medical Writing contributes to Cardinal Health_** The Medical Writing Project Manager is a member of the Medical Affairs team, within in Global Medical Products, and is responsible for the planning, development, writing and reviewing Post Market Surveillance Plans and Clinical Evaluation Reports for the medical devices. The Project Manager
Job Source: Cardinal HealthCardinal Health
Phoenix
The Scientific Communications and Strategy team within Cardinal Health Marketing & Engagement drives the creation of high-quality documents and strategic insights that contribute to the overall success of our business. Our team of scientists, writers, and graphic designers collaborate with internal business units and Pharma/Biotech clients to condu
Job Source: Cardinal HealthGrammarly
Scottsdale, AZ, United States
We’re looking for a writing expert freelancer. As a writing expert freelancer, you will revise user-submitted texts for correctness (e.g., grammar, spelling, punctuation). We’re looking for someone who Has 2+ years of editing experience Speaks and writes English skillfully and has an excellent grasp of English grammar and communication Prioritizes
Job Source: GrammarlyGrammarly
Glendale, AZ, United States
We’re looking for a writing expert freelancer. As a writing expert freelancer, you will revise user-submitted texts for correctness (e.g., grammar, spelling, punctuation). We’re looking for someone who Has 2+ years of editing experience Speaks and writes English skillfully and has an excellent grasp of English grammar and communication Prioritizes
Job Source: GrammarlyGrammarly
Phoenix, AZ, United States
We’re looking for a writing expert freelancer. As a writing expert freelancer, you will revise user-submitted texts for correctness (e.g., grammar, spelling, punctuation). We’re looking for someone who Has 2+ years of editing experience Speaks and writes English skillfully and has an excellent grasp of English grammar and communication Prioritizes
Job Source: GrammarlyArizona State University
Tempe, AZ, United States
Director, Writing Services page is loaded Director, Writing Services Apply locations Tempe, AZ time type Full time posted on Posted 6 Days Ago job requisition id R899 Director of Writing Services The ASU Foundation (ASUF) fosters partnerships between ASU and like-minded individuals, corporations and foundat
Job Source: Arizona State UniversityScottsdale, AZ, United States
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.
We are looking for consultants interested in joining our extended team!
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
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Senior Medical Writing Consultant jobs in Scottsdale, AZ, United States
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