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 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 in Global Health & Pharma’s international awards programs for the last three consecutive years. For more information, visit or follow MMS on LinkedIn. Responsibilities Under minimal supervision, 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 and maintain timelines and workflow of writing assignments. Practice good internal and external customer service. Be highly proficient with styles of writing for various regulatory documents and client templates & style guides. Interact directly and independently with clients to coordinate all facets of projects; demonstrate competent communication skills for projects. Contribute substantially to, or manage, 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 Bachelor’s, Masters, or PhD Degree in scientific, medical, clinical discipline, or related field is required with at least 6 years of previous regulatory writing experience; Masters or PhD degree is preferred. Substantial Oncology experience required. Substantial clinical study protocol experience as lead author is required. Experience leading and managing teams while authoring regulatory documents with aggressive timelines. Experience in regulatory submissions (clinical study reports) presented to regulatory authorities is a plus. Understanding of clinical data is essential. 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 is preferred. Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines is a plus. Not required, but experience with orphan drug designations and PSP/PIPs is a plus. #J-18808-Ljbffr MMS

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