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 at Avalere Health producing editorial content to support healthcare communication goals. Collaborating with teams to deliver quality projects on time and within budget.
Clinical Writer preparing regulatory and clinical documentation for innovative medical devices at Withings. Collaborating with technical teams and ensuring compliance with medical regulations.
Medical Writer at Kintiga preparing AMNOG and JCA dossiers, supporting strategic planning and G - BA consultations. Focused on quality deliverables using expertise in the healthcare and life sciences sector.
Medical Writer preparing clinical regulatory documents in collaboration with client teams. Contributing to the production of high - quality regulatory documentation for the international pharmaceutical industry.
Senior Medical Writer leading complex writing projects and managing writing activities at Syneos Health. Collaborating with medical teams while adhering to regulatory standards.
CDI Specialist reviewing medical records and facilitating documentation improvement at Ensemble Health Partners. Requires acute care nursing experience with a focus on Pediatric/NICU.
Manager overseeing Clinical Documentation Improvement (CDI) program and staff at multiple Illinois locations. Ensuring accurate documentation and coding practices while collaborating with healthcare professionals.
Medical Writer II providing strategic writing expertise for Clinical Evaluation Reporting documents at Abbott. Collaborating on clinical evaluation projects for medical devices across multiple sites.
Principal Medical Writer managing major client accounts at Madano, delivering strategic, scientifically rigorous content and overseeing a scientific services team.
Senior Medical Writer creating scientifically robust communications for healthcare. Collaborating with cross - functional teams to drive impactful content delivery.