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Certara USA, LLC A 1895 - Sr. Regulatory Writer - Clinical Team in Malvern, Pennsylvania

Reference #: 1895Certara is hiring a Senior Regulatory Writer to join our Synchrogenix Division! This position can be based out of any US Certara office, or full time remote.Certara is the global leader in advancing modern, efficient drug development.We provide proven modeling and simulation, regulatory and real-world value assessment software platforms and services. In partnership with our clients, we help reduce clinical trial burden, accelerate regulatory approval and increase patient access to medicines.Synchrogenix, a Certara Company: Achieving Regulatory SuccessAs Certara's Regulatory Science division, Synchrogenix accelerates the regulatory submissions of medical innovations worldwide through customized regulatory solutions, including strategy, communications, operations and technology. Synchrogenix is comprised of some of the most respected talent in the industry, including thought leaders, writers and editors, and regulatory submissions specialists. Our people are talented, quality-minded, and client and stakeholder-oriented.Synchrogenix's people are at the core of our success, and our most successful people are:collaborative and value being part of a teamexperts with a thirst for continued learningconsultativewith an ability to articulate process and expertisedeadline-driven and able to operate in a fast-paced environmentJob Overview:Regulatory Writers prepare high quality documentation for regulatory submissions in order to help streamline the regulatory approval process for our clients. The Senior Regulatory Writer (SRW) is a major contributor to document authorship for a variety of documents across different service lines. The SRW will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. Synchrogenix is looking for individuals looking to use their expertise in clinical regulatory writing to lead teams and help clients achieve their goals.Responsibilities:* Lead or participate in a project team which may be led by a Principal Regulatory Writer or Associate Principal Regulatory Writer* Author documents per client specifications, templates, style guides, and other guidance documents* Author documents per regulatory authority guidelines and requirements* Act as client advisor, working with all parties to lead development of strategies for organizing and preparing regulatory documents* Practice blameless problem solving, taking broad perspectives in resolving issues to prevent negative impact to work* Manage budget for a low complexity project, including all contributors (writers, editors)* Usher documents through the review process, conduct comment resolutions meetings (CRMs), and successfully lead a project team to consensus* Maintain collaborative, proactive, and effective communication with both client and internal teams* Lead or participate in project-related meetings and teleconferences* Provide coaching to junior staff for study level documentsEducation, Experience, Training, and Knowledge:* Bachelor's degree* 3-5+ years of regulatory writing experience or equivalent experience with clinical related documentation* Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance* Experience in the development of submission-level documents (does not require functioning as a document lead)* Experience in the development of clinical documents such as Clinical Study Reports, Investigator Brochures, protocols ISS and/or ISESkills and Abilities:* Intermediate proficiency with Microsoft Word skills (editing tools, creating and modifying tables and inserting figures) and document management techniques* Strong understanding of the document creation process and of the drug development lifecycle* Able to synthesize data across multip