New hires based in the US will be required to demonstrate that they have been fully vaccinated for COVID-19 or qualify for a medical or religious exemption or accommodation to this vaccination requirement, subject to applicable law. Job openings at Alimentiv, view positions and submit a general application Current Opportunities Working at Alimentiv At Alimentiv, our mission is to Transform Human Health. Occasional business travel may be necessary. Management of external resources preferred.Įxcellent verbal and written communication skills with the ability to effectively communicate with a variety of teams and individuals. Works collaboratively with functional contributors (Clinical Development, Pharmacovigilance, Biometrics, Regulatory Affairs, Regulatory Operations, others), ensuring all source information and data are appropriately reported in terms of accuracy, completeness, and scientific interpretation, and in accordance with project timelines.Īssists with the coordination of the compilation of final documents and appendices provided by other functions.Ĭontributes to development of document and process standards, template development, and other aspects of document management.Īssists with the management of external vendors or consultants to ensure document compliance with guidelines, as well as quality and adherence to timelines.Ĭontributes to other non-regulatory writing activities as needed.īA / BS and 10+ years Regulatory Writing experience, or MA / PhD and 8+ years of experience.Įxtensive experience in clinical-regulatory documents authoring to prepare clinical / regulatory documents as described above. 2,198 Medical Writing jobs available in Naval Medical Center San Diego, CA on.
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MEDICAL WRITER JOBS SAN DIEGO PROFESSIONAL
Leverage your professional network, and get hired. Participates in regulatory teams, providing advice / guidance to the team on regulatory document requirements and optimal presentation of data.Īssists with the management of document timelines / resource planning. Today’s top 21 Medical Writer Senior Medical Writer jobs in San Diego, California, United States.
Represents Regulatory Writing on cross-functional project teams. 60,000 - 70,000 a year Full-time Monday to Friday + 1 Or bachelors level scientist with 2-3 years’ experience in medical communications, medical/clinical lab or pharmaceutical environment. Plans, develops, and / or provides oversight of clinical / regulatory documents, such as CSRs of all phases, Investigator Brochures, CTD summaries, PIPs, briefing packages, responses to agency questions, and other document types as needed, according to ICH guidances, regulatory requirements and internal document standards. This position will be located in Palo Alto, CA and reports to the Sr.ĭirector, Global Regulatory Communication. The Director, Regulatory Writing plans, authors and manages regulatory / clinical documents to support clinical development programs and regulatory submissions.Īssists with the management of external resources to prepare regulatory / clinical documents. The job offer you are looking for is no longer available.
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