REMOTE Senior Medical Writer US Residents only

Individual has authored, CSRs & Amendments, over 10+ is a must Senior Medical Writer - Base Salary adjusts according to COLA of work residence. What is presented is highest range reflecting the Bay Area/NYC/Cambridge. Base Salary - USD $142,100 to $195,360, who knows, perhaps more We have a great relationship with this client, I will get you an interview If you are a perfect fit, then; Please call my land line, 860 889 4141 until 8PM EST 7 days a week as you can take notes & after you email a word docx resume to me [email protected] 7+ to 10 years experience Seniority Level - Mid-Senior Minimum Education - Bachelor's Degree Screening Questions, Individual has authored, CSRs & Amendments, over 10+ Ideal Candidate, extremely seasoned clinical studies Phase 1-3 medical writer. Focus more on clinical science, CSR documentation excellence over safety. Must be author, not editor nor team manage nor project team lead. Person writes 75%+ of their time with focus on CSRs. Biotech/Pharma strongly preferred. CROs considered. Med Device - Diagnostic: considered though low viability ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES: Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.) Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries). Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Represents Global Medical Writing at cross-functional team meetings (e.g., study team, development team, other sub teams). Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met. Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments Adheres to departmental procedures and practices and technical and industry standards during all aspects of work. Works effectively with cross-functional groups within the company Other tasks as assigned. SCOPE: This position progressively develops the medical writing function in alignment with the requirements of the Development Sciences department and organizational goals. Filling this need with a regular full-time employee will enable the company to reduce writing-related CRO and contractor costs, increase Global Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. EXPERIENCE: Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility. 1) Medical Writing: Experience writing, reviewing, or editing protocols and clinical study reports required. Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred. Experience writing, reviewing, or editing regulatory briefing books preferred. Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content. Ability to interpret and create complex tabular and graphical clinical data presentations. Advanced applied knowledge of basic clinical laboratory tests. Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug). 2) Clinical Studies Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets. Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection. Intermediate to advanced applied knowledge of: o documentation required for the conduct of clinical studies o protocol design (including objectives, efficacy and safet