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MMS

The difference is in the data.

Senior ICF Writer

Medical writerMedical writerFull TimeRemoteSeniorTeam 501-1,000H1B SponsorCompany SiteLinkedIn

Location

United States

Posted

68 days ago

Salary

0

Seniority

Senior

No structured requirement data.

Job Description

Senior ICF Writer

MMS

Role Description - 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, Informed Consent Forms and Clinical Protocols. - 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 communication 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. Qualifications - 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. - Oncology, General Medicines, Infectious Diseases and Vaccine experience preferred. - Substantial informed consent and clinical study protocol experience, as lead author, required. - Experience leading and managing teams while authoring regulatory documents with aggressive timelines. - Experienced in understanding complex clinical information. - Translate complex medical and scientific information into clear, patient-friendly language. - Experienced in collaboration and cross-functional communication. - 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. - Not required, but experience with orphan drug designations and PSP/PIPs a plus.

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