Scientific Publication Medical Writer at Gilead developing materials for peer-reviewed publications in Viral Hepatitis, Chronic Liver Diseases, and Inflammation. Collaborating with research teams to ensure compliance with publication guidelines and high standards.
Responsibilities
Collaborate with cross-functional teams to develop Viral Hepatitis, Chronic Liver Diseases, and Inflammation related publications
Write, edit, and proofread scientific content for publication in peer-reviewed journal, conference presentations with a focus in topics
Join forces with cross-functional leads to identify clear and scientifically appropriate ways to communicate Gilead Science data
Conduct literature searches and gather relevant data to support scientific arguments and conclusions
Ensure compliance with publication guidelines and ethical standards (e.g., ICMJE, GPP, CONSORT)
Manage multiple projects simultaneously and meet deadlines in a fast-paced environment while maintaining a high level of quality and accuracy
Work closely with key stakeholders, including researchers, clinicians, and to ensure accurate interpretation and communication of scientific data
Stay current with developments in the research, including new therapies, treatments, and regulatory changes, and communicate relevant information to internal teams
Understand the evolving publications landscape through engagement with and participation in professional societies (e.g., ISMPP)
Working knowledge of publication databases (e.g. Datavision or similar)
Requirements
10+ Years with BS/BA OR 8+ Years with MS/MA or MBA
Advanced degree in a scientific or medical discipline (Ph.D., MD, PharmD) including 5-8 years’ experience supporting publication development
Some specialized training in Viral Hepatitis, Chronic Liver Diseases, and Inflammation preferably within the pharmaceutical industry
Clear understanding of current publication environment, good publication practices, Sunshine Act/Pharma Code of Conduct, ICMJE, GPP4, and other global guidelines related to publications, scientific data communication, and transparency standards
Proficiency in Microsoft Office suite and reference management software
Strong attention to detail and ability to critically analyze data and scientific literature
Familiarity with publication planning processes, including authorship criteria, disclosure requirements, and journal and congress submission guidelines
Strong organizational skills and ability to work independently
Benefits
company-sponsored medical, dental, vision, and life insurance plans
discretionary annual bonus
discretionary stock-based long-term incentives (eligibility may vary based on role)
Senior Medical Writer overseeing high - quality clinical and regulatory documents at Ipsen, a biopharmaceutical company. Leading cross - functional teams and contributing to regulatory strategy while ensuring compliance and innovation in medical writing practices.
Medical Writer I role focusing on document management within Veeva systems for clinical projects. Supporting compliance and adherence to GxP guidelines while collaborating with stakeholders.
Medical Copywriter creating pharmaceutical promotional content for a global digital agency. Developing strategies and overseeing editorial quality for marketing communications in the life sciences sector.
CDI Nurse assisting GBMC Health Partners with documentation improvement efforts. Collaborating with physicians and clinicians on patient records and risk management.
Clinical Documentation Specialist working with healthcare teams to ensure accurate medical record documentation. Aiding in compliance and coding education for clinical documentation improvement.
Medical Writer at Real Chemistry developing scientific copy for healthcare communications. Collaborating with medical writers and adhering to style guidelines for various projects.
Clinical Documentation Specialist responsible for receiving and processing healthcare documentation requests. Analyzing and validating requests while ensuring compliance with regulations and organizational standards.
Senior Medical Writer shaping key clinical and regulatory documents at Thermo Fisher Scientific. Collaborating with teams to drive strategy, quality, and execution of early - phase programs.
Medical Writer I ensuring data integrity and quality checks for clinical documents in a biopharmaceutical company. Collaborating with medical writing teams and participating in stakeholder meetings.