Senior Medical Writing Consultant - Europe

MMS Holdings Inc; Catania; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

MMS Holdings Inc., a leading CRO, is seeking a full-time Medical Writer to undertake critical evaluations and write clinical documents. The role requires strong writing skills, regulatory experience, and the ability to manage projects independently. This is an excellent opportunity to join a dynamic team focused on delivering high-quality submissions for the pharmaceutical industry.

Competenze

• At least 3-5 years of regulatory and clinical medical writing experience.
• Experience leading and managing project teams.
• Exceptional writing and organizational skills.

Mansioni

• Critically evaluate and interpret medical literature for study design.
• Write and edit clinical development documents including protocols and reports.
• Mentor medical writers and manage writing assignments.

Conoscenze

Writing Skills

Organization

Communication

Team Management

Regulatory Understanding

Formazione

Bachelor's, Master's, or Ph.D. in scientific or clinical discipline

Strumenti

MS Word

Excel

PowerPoint

Descrizione del lavoro

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

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