Senior Medical Writing Consultant
4 settimane fa
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 or follow MMS on LinkedIn . We are looking for full time 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, 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 #J-18808-Ljbffr
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Senior Medical Writing Consultant
4 settimane fa
Roma, Italia MMS Holdings Inc. A tempo pienoMMS 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...
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Director, Medical Writing
2 giorni fa
roma, Italia Altro A tempo pienoA global healthcare company is seeking a Director of Medical Writing based in Italy. This role requires strong oversight of medical writing deliverables and leadership of a team focused on regulatory submissions. Ideal candidates will have significant experience (10+ years) in the pharmaceutical space, with expertise in IND/CTA and NDA/MAA. This position...
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Senior Pcb Layout Engineer
2 settimane fa
Roma, Italia Natus Medical Incorporated A tempo pieno 90.000 €A leading medical equipment manufacturer is seeking a Senior Design Engineer to manage PCB layout design for advanced medical systems. The ideal candidate will lead multi-layer PCB design using Altium Designer, collaborating across teams to ensure adherence to performance and compliance standards. Candidates should possess at least 7 years of experience in...
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Senior Consultant
3 settimane fa
Roma, Italia Cattaneo Zanetto Pomposo & Co. A tempo pienoOverviewThe Senior Consultant will work closely with the Partner and the Director of the relevant practice of the firm. In particular, they will manage projects of advocacy, lobbying and coalition building. The Senior Consultant is required to monitor the legislative, regulatory and policy activity of the main Italian government bodies and regulatory...
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Senior Consultant
2 settimane fa
Roma, Italia Cattaneo Zanetto Pomposo & Co. A tempo pieno 90.000 €Overview The Senior Consultant will work closely with the Partner and the Director of the relevant practice of the firm. In particular, they will manage projects of advocacy, lobbying and coalition building. The Senior Consultant is required to monitor the legislative, regulatory and policy activity of the main Italian government bodies and regulatory...
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Senior consultant
2 settimane fa
Roma, Italia Cattaneo Zanetto Pomposo & Co. A tempo pienoOverview The Senior Consultant will work closely with the Partner and the Director of the relevant practice of the firm. In particular, they will manage projects of advocacy, lobbying and coalition building. The Senior Consultant is required to monitor the legislative, regulatory and policy activity of the main Italian government bodies and regulatory...
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Senior PCB Layout Engineer
2 settimane fa
Giuliano di Roma (FR), Italia Natus Medical Incorporated A tempo pienoA leading medical equipment manufacturer is seeking a Senior Design Engineer to manage PCB layout design for advanced medical systems. The ideal candidate will lead multi-layer PCB design using Altium Designer, collaborating across teams to ensure adherence to performance and compliance standards. Candidates should possess at least 7 years of experience in...
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Senior Consultant
1 settimana fa
giuliano di roma, Italia Cattaneo Zanetto Pomposo & Co. A tempo pienoOverviewThe Senior Consultant will work closely with the Partner and the Director of the relevant practice of the firm. In particular, they will manage projects of advocacy, lobbying and coalition building. The Senior Consultant is required to monitor the legislative, regulatory and policy activity of the main Italian government bodies and regulatory...
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Senior Consultant
2 giorni fa
giuliano di roma, Italia Cattaneo Zanetto Pomposo & Co. A tempo pienoOverviewThe Senior Consultant will work closely with the Partner and the Director of the relevant practice of the firm. In particular, they will manage projects of advocacy, lobbying and coalition building. The Senior Consultant is required to monitor the legislative, regulatory and policy activity of the main Italian government bodies and regulatory...
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Medical Doctor
4 settimane fa
roma, Italia Crossing Hurdles A tempo pienoBase pay range$90.00/hr - $160.00/hrType: Hourly contractLocation: RemoteCommitment: 10–40 hours/weekRole ResponsibilitiesTranslate, adapt, and structure complex medical concepts into clear, AI-ready rubrics and training materials.Produce accurate, culturally nuanced medical content reflecting real‑world Italian healthcare practice.Write fluently in...
