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)
Clinical Documentation Specialist at OhioHealth reviewing inpatient medical records for severity of illness and risk of mortality. Collaborating with providers to enhance clinical documentation accuracy in a supportive environment.
Clinical Documentation Specialist ensuring accuracy and completeness of clinical documentation for healthcare providers. Collaborating with medical staff to meet compliance and regulatory standards.
CDI Specialist facilitating patient clinical documentation improvement at Ensemble Health Partners, enhancing accuracy in patient records. Collaborating with healthcare providers for optimal care documentation completion.
Clinical Documentation Sr Registered Nurse RN responsible for reviewing medical records and education of physician documentation guidelines. Involves collaboration with healthcare teams and regulatory adherence.
Analyst/Medical Writer conducting detailed data analysis from clinical trials at Costello Medical. Engaging collaboratively on various projects while developing strong scientific and writing skills in healthcare communications.
Medical Writer contributing to the Clinical Evaluation reporting for Abbott's medical devices. Collaborating with cross - functional teams to produce regulatory submissions with attention to detail.
Senior Medical Writer at Syneos Health translating insights into outcomes in medical writing. Collaborating to simplify work while leading medical writing projects within the biopharmaceutical industry.
Consultant/Medical Writer generating compelling dossiers and value communications for ICON plc. Collaborating with multidisciplinary teams to shape the future of clinical development in the pharmaceutical industry.
Principal Medical Writer delivering complex clinical documentation for regulatory submissions in a biopharma company focused on innovative health solutions.