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.Highly proficient with styles of writing for various regulatory documents.Practice good internal and external customer service.Leverage your professional network, and get hired. Maintain timelines and workflow of writing assignments Today’s top 122 Mms Holdings Inc Medical Writer jobs in United States.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, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, 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.For more information, visit or follow MMS on LinkedIn. 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. 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. 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.
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