Role Description We are currently recruiting for a detail-oriented, team-focused Medical Writer with a focus in document quality control (QC). In this role, you will support Lexicon across multiple functional areas including: - Clinical Operations - Medical Affairs - Regulatory Affairs - External Affairs - CMC teams Your responsibilities will include: - Collaborating with functional areas to write, review, and QC documents including clinical study reports, protocols, Investigator Brochures, publications, presentations, and other clinical/regulatory documents for clarity, brevity, and consistency with the overall development program and source documents. - Driving the document development process for the functional review team, including using medical writing templates and document management software (e.g., StartingPoint and Veeva Vault). - Synthesizing clinical data, information, references, and other sources with input from SMEs program team members to prepare and present data and document messaging consistent with regulatory requirements, guidelines, and program strategy. - Reviewing and QCing documents. - Creating and managing document timelines. - Attending project-related meetings. - Assisting team members with document locations. - Developing and maintaining a Lexicon Style Guide. - Collaborating with vendors, which may include vendor oversight. - Identifying and appropriately communicating or escalating risks associated with document delivery or other writing-related issues. - Completing project-specific and company training, as assigned. Qualifications - Bachelor’s degree in healthcare or writing-related field required. - 5+ years technical or regulatory writing and/or QC experience; 2+ acceptable if in medical or regulatory writing. - Excellent QC skills. - Excellent writing and editing skills. - Excellent attention to detail—style, consistency, grammar, syntax, scientific accuracy. - Excellent interpersonal and oral communication skills. - Ability to communicate with professionals from a variety of backgrounds. - Strong knowledge of MS Word, Excel, PowerPoint, and Outlook. - Ability to prioritize multiple projects. - Project/time management and organizational skills, as well as the ability to work independently. - Flexibility in meeting challenging deadlines and changing requirements while working on multiple projects. - Comprehensive Microsoft Office skills, especially Word but also PowerPoint and Excel, as well as internet skills. - Knowledge of current requirements and guidelines applicable to submission documents. Company Description Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transform patients’ lives. Through our unique approach to gene science based on Nobel Prize-winning technology, we are moving forward rapidly to bring innovative therapies to market. At Lexicon, our passion and dedication is driven by the patients for whom we work. Lexicon employees are inspired by the idea that their work can improve patients' lives and we know that our employees are essential to the success of our mission. Every day they bring their passion, talents and dedication to an engaging environment where they are rewarded with opportunities to realize their potential. We are dedicated to making Lexicon a great place to work by providing employees with the benefits, services, and programs as part of our total rewards package. For additional information about Lexicon and its programs, please visit www.lexpharma.com . Lexicon is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran. Lexicon Pharmaceuticals, Inc. is a drug-free workplace. Candidates are required to pass a drug test, background check, driving check (if applicable) and verification of credentials before beginning employment.

• writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences • demonstrates a command of relevant therapeutic areas and expertise with assigned products • analyzes, interprets, and applies clinical data to produce high-quality scientific communications • follows all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices

• Manage and facilitate anonymization of datasets and documents against planned timelines, in accordance with Incyte SOPs and regulatory requirements. • Assess documents in-scope for public disclosure according to EMA Policy 0070 and Health Canada PRCI. • Work closely with Biostatistics and Programing groups and Medical Writing teams to identify and assimilate the required documents and datasets. • Develop anonymization plans based on direct and indirect identifiers by measuring and mitigating re-identification risk according to GDPR guidance. • Process datasets and documents and apply required transformations. • Contribute to Anonymization Reports to support anonymization packages for policies of Health Canada and EMA. • Ensure accurate and consistent redaction of clinical trial documents to support EU CTR, ClinicalTrials.gov, and Publications. • Quality check of documents redacted/anonymized by other team members. • Collaborate with Regulatory Operations to ensure the publishing of redacted documents in the Regulatory Document Management System. • Experience with the use of Technology Tools for delivery of Anonymized Clinical Documents. • Assist in the development of internal work instructions, training materials, and procedures as needed to comply with global requirements and Incyte policies. • Ability to work with minimum supervision and resolve issues. • Develop and maintain collaborative relationships internally to ensure effective and efficient working relationships and the delivery of high quality deliverables. • Stay informed of new clinical trial disclosure and transparency requirements globally, including but not limited to clinical trial registration and posting of results.

Role Description The Medical Writer will leverage scientific/clinical expertise and exceptional medical writing skills to support development of Medscape Medical Affairs programs delivered at the highest standards. Key Responsibilities - Create high-quality scientific, medical, and/or clinical content for physicians, nurses, pharmacists, and other healthcare providers. - Develop PowerPoint presentations, text-based copy, and other project-related deliverables for multimedia programs across digital, live virtual, and/or in-person formats. - Ensure content alignment with program goals and client expectations. - Engage with thought leaders and medical experts in the specified therapeutic area to support content development. - Maintain up-to-date knowledge of key clinical issues within the therapeutic areas of interest; remain current with relevant literature; clinical practice guidelines; approved therapeutic drugs, regimens, and devices; and therapeutic pipelines. - Create medical education content that is clinically appropriate, instructionally-sound, and adherent to industry regulations. - Support application of adult learning theory, instructional design principles, and best practices for health care provider education for specified projects. - Meet regularly with team members to review work quality, client satisfaction, productivity metrics, and progress toward project-related objectives. - Demonstrate accountability against defined performance standards for working with internal teams and clients. - Complete projects within established timelines and to specifications. Qualifications - Minimum 3 to 5 years’ experience in developing digital, live virtual, in-person, and hybrid medical education programs for healthcare providers. - At least 3 to 5 years’ experience as a medical writer/content developer at a medical education/communications AGENCY. - Preference given to individuals with prior Medical Affairs experience. - Preference given to individuals with established expertise in hematology/oncology, neurology, or immunology. - Highly proficient in written English and verbal communication skills; additional languages a plus. - Highly proficient with Microsoft Office suite - particularly PowerPoint - with excellent editorial skills (writing and editing). - An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; minimum of a Bachelor of Science degree (life sciences, public health, or clinical sciences) or similar with several years’ relevant work experience required. Requirements - Excellent computer skills that include working remotely on shared networks and cloud-based systems (e.g., SharePoint, Google Drive, Workfront, and others). - Proficiency with web-based data and document sharing sites and authoring tools (Box, Read Cube, EndNote, Tableau) a plus. - Comfortable in a highly deadline-driven environment; able to pivot quickly between tasks and adapt to rapidly shifting priorities. - Self-motivated and capable of working independently. - Possessing strong problem-solving and time-management skills; capable of addressing unforeseen issues to ensure that project goals and timelines are consistently met. - High degree of professionalism and comfortable building collaborative work relationships with both internal and external stakeholders. - Excellent organizational skills, with a track record of meeting deadlines. - Willingness to travel; estimated up to 15% (during peak times) for program delivery and training opportunities. Benefits - Health Insurance (medical, dental, and vision coverage). - Paid Time Off (including vacation, sick leave, and flexible holiday days). - 401(k) Retirement Plan with employer matching. - Life and Disability Insurance. - Employee Assistance Program (EAP). - Commuter and/or Transit Benefits (if applicable). - Eligibility for specific benefits may vary based on job classification, schedule (e.g., full-time vs. part-time), work location and length of employment. Salary Range $82,500 - $90,000 Depending on Experience.