
501 - 1000 employees
Founded 2007
đ§Ź Biotechnology
đ Pharmaceuticals
âïž Healthcare Insurance
Biotechnology âą Pharmaceuticals âą Healthcare Insurance
TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.
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501 - 1000 employees
Founded 2007
đ§Ź Biotechnology
đ Pharmaceuticals
âïž Healthcare Insurance
Biotechnology âą Pharmaceuticals âą Healthcare Insurance
TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.
âą Perform data/referencing quality check of scientific/medical assets âą Review content and identify any non-compliances with local regulatory guides âą Perform actions in the Review and Approval platform (Veeva Vault) âą Check anchors/links to references required for scientific/medical assets âą Identify assets that may require pre-alignment with internal stakeholders âą Flag claims that may be difficult to substantiate or do not follow guidelines âą Track asset quality data for internal and external reporting
âą Experienced Medical Writer or Medical Content Reviewer (3-5 years) âą Scientific background and degree (PharmD, MD, PhD or Masters) âą At least 3 years producing or reviewing content for Pharma/Biotech industry âą Excellent medical writing skills âą Strong attention to detail and accuracy âą Ability to manage and prioritize multiple activities âą Good communication, coordination and time management skills âą Fluent in oral and written English AND Portuguese âą Ability to work within a team or across multiple teams âą Values teamwork and collaboration, diversity and inclusion, and innovation
âą Opportunities for personal and professional growth âą Collaboration and innovation âą Valuing teamwork and inclusion
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