![]() The ideal candidate would hold a Bachelors, Masters, or Ph.D.Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience.At least 3 years of previous experience in the pharmaceutical industry.Mentor medical writers and other members of the project team who are involved in the writing process.Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary. ![]() Contribute substantially to, or manages, production of interpretive guides.Interact directly and independently with client to coordinate all facets of projects competent communicator skills for projects.Expert proficiency with client templates & style guides Draft original content and work with existing content to improve readability, including working with content management systems and structured authoring tools.Highly proficient with styles of writing for various regulatory documents.we prioritize hiring top talent and cultivating a culture based on merit. Practice good internal and external customer service competitive salaries, comprehensive health benefits and equity packages.Maintain timelines and workflow of writing assignments.Complete writing assignments in a timely manner.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, presentation materials and publications to medical journals.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.Apply to Technical Writer, Proposal Writer, Writer/editor and more Skip to main content. 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 in Global Health & Pharma’s international awards programs for the last three consecutive years.įor more information, visit or follow MMS on. 15 Specification Writer jobs available in Dallas, TX on. Learn more about careers with USAA and view jobs here. 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. Wherever you are in your career, you can join our team serving those who serve and their families. ![]() Whether its our comprehensive healthcare coverage, coveted employee. ![]() 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. Search for vacancies at any of the PlayStation sites and take your career to the. This job offer is not available in your country. ![]()
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