Remote Associate Director, Medical Writing

LEXICON PHARMACEUTICALS; Bridgewater Township (NJ); Remote; USD 175,000 - 195,000; Full time

Job summary

Lexicon Pharmaceuticals, Inc. is seeking a collaborative, agile Senior Medical Writer to support the R&D and Quality/Regulatory groups, producing accurate, concise, compliant documents and acting as a subject-matter expert on writing processes and style guides.

The role is based in Bridgewater, NJ, The Woodlands, TX, or remote. Responsibilities include coordinating cross-functional teams, integrating data into reports and journal submissions, leading reviews of protocols and study reports, and

Qualifications

• Bachelor’s Degree in a scientific/healthcare field in which writing is a major component is required
• AMWA membership and ELS certification is a plus
• Minimum of five (5) years of medical writing experience in a CRO, medical communications company, pharmaceutical company or other medical/scientific setting
• Knowledge of the drug development and approval processes in the U.S. is required
• Prior experience authoring publications, protocols, CSRs, Non-clinical reports and related documents; IND and NDA modules and summaries and other regulatory documents
• Experience with oversight of external Medical Writers and deliverables is required
• Skilled and adept with Microsoft Word, Microsoft SharePoint, Endnote, Adobe Acrobat

Responsibilities

• Guiding and coordinating cross-functional collaborations with key company stakeholders to develop research, quality and regulatory documents
• Helping to integrate chemistry, manufacturing, non-clinical and clinical trial information and data into concise and compelling reports and summaries (conference presentations, abstracts, posters, and slides) and journal manuscript submissions
• Leading writing, editing, and cross functional review of clinical protocols, amendments, and clinical study reports, ensuring accuracy, clarity, completeness, and compliance with established formatting, content and style guidelines
• May serve in an oversight role in the assembly and/or QC of final study reports
• Overseeing external contractors including CROs in the authoring of Lexicon documents, including preparing concise and unambiguous requirements statements or SOWs
• Ensuring process consistency with Lexicon SOPs and applicable Lexicon standards for completeness, degree of detail, quality (including data accuracy) and style/formatting according to pre-agreed timelines
• Assisting in the development and maintenance of procedures and supporting documentation for the creation, review, and approval of documentation of Lexicon research activities, including, but not limited to, SOPs, templates, Word toolbars, work practices, best practices training guides and aids for Lexicon authors and reviewers
• Serving as the Protocol Review Committee (PRC) Coordinator, to ensure that all PRC-related materials are efficiently collected, reviewed, finalized, and retained according to Lexicon SOPs
• Serving as the Clinical Data Review Committee (CDRC) Coordinator
• Ensuring that all final versions of documents are filed in secure network locations, and, where needed, version controlled with correct access permissions and security
• Serving as a subject matter expert on processes and tools for organizing, writing, editing and reviewing research, development, quality and regulatory documents
• Maintaining, updating and providing training on the Lexicon Style Guide for authors and the Lexicon Reviewer Guide for reviewers
• Estimated Allocation of Effort: Authoring of documents: 40%, Reviewing of documents: 40%, Training: 10%, Other: 10%

Job description

Lexicon Pharmaceuticals, Inc. is seeking a collaborative, agile Senior Medical Writer to support the R&D and Quality/Regulatory groups, producing accurate, concise, compliant documents and acting as a subject-matter expert on writing processes and style guides.

The role is based in Bridgewater, NJ, The Woodlands, TX, or remote. Responsibilities include coordinating cross-functional teams, integrating data into reports and journal submissions, leading reviews of protocols and study reports, and