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Farmaceutisch field project | Projectcontract tot eind 2027 Heb je ervaring in de farmaceutische wereld en wil je jouw terreinervaring een nieuwe dimensie geven? Voor een nieuw farmaceutisch project rond de begeleiding van apotheken en de verbetering van het patiëntentraject bi
Join a global healthcare leader where innovation, purpose, and professional growth come together. At IQVIA, you'll gain exposure to leading pharmaceutical and biotechnology organizations, diverse therapeutic areas, cutting-edge technologies, and meaningful work that helps improve
At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate increasingly complex regulatory environments and accelerate patient access to innovative therapies. We are seeking an experienced Associate Director, Regula
- 現在3名(女性3名)。年齢層は30代前半〜後半。 - 多様なバックグラウンドを持つメンバーが、それぞれの強みを活かして活躍。 -コミュニケーションを大切にし、意見交換やサポートが自然に行われる風通しの良い環境の中、各自が高い責任感を持ち、期限を守って着実に業務を遂行しており、新しいメンバーも安心して馴染めるようフォロー体制を整えています。 - 治験薬臨床試験患者検体における血液学的検査、尿一般検査(鏡検含む)、凝固検査等の臨床検査業務およびPBMC(末梢血単核細胞)
At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and support the successful development, approval and lifecycle management of healthcare products. We are seeking an experie
Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) models offer the best of both worlds: the opportunity to work as an integrated member of a leading sponsor's team while benefiting from the global expertise, ca
For candidates able to start before December 2026, a discretionary sign‑on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience. Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA,
- Responsável por construir e sustentar a plataforma corporativa de dados, garantindo que informações críticas estejam disponíveis, confiáveis e escaláveis para suportar decisões de negócio, analytics avançado e iniciativas de IA; - Desenvolver e manter pipelines de dados e integ
Job Overview Manage the contract strategy and support delivery of all required start-up contracting activities for selected sponsors and for complex studies or multi-protocol programs as determined by the Sponsor’s requirements. May include line management responsibilities. Esta
MCRA, an IQVIA business, is a medical device advisory firm and clinical research organization. Through integrated regulatory, clinical research, reimbursement, healthcare compliance, and quality capabilities, the organization supports medical technology clients from concept throu
◆Hiring Managerからのメッセージ 本ポジションは、医療ビッグデータやリアルワールドデータ(RWD)を活用し、自治体・医療機関向けのプロダクト/ソリューション開発をリードするポジションです。国内外のIQVIAグループや多様な専門家と連携しながら、医療・ヘルスケア領域における新たな価値創出を推進していただきます。 ・医療情報システムの開発や導入経験を活かして社会課題解決に取り組みたい方 ・医療データやリアルワールドデータを活用した新規ソリューション開発に興味がある方 ・プロダクトマネジメントやプロジェ
Job Overview Under moderate supervision, executes the feasibility, site identification regulatory and start-up activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotia
Location: France Work Model: Hybrid or Homebased Make an impact on patient health with IQVIA! Join our Global Site Activation Team, a 2,000‑strong network driving high‑quality site activation and ensuring patients gain access to safe and effective treatments. We lead with innova
We are seeking Associate Scientist, Sample Preparation to join IQVIA Laboratories at Ithaca. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform
Join a global healthcare leader where innovation, purpose, and professional growth come together. At IQVIA, you'll gain exposure to leading pharmaceutical and biotechnology organizations, diverse therapeutic areas, cutting-edge technologies, and meaningful work that helps improve
Join a global healthcare leader where innovation, purpose, and professional growth come together. At IQVIA, you'll gain exposure to leading pharmaceutical and biotechnology organizations, diverse therapeutic areas, cutting-edge technologies, and meaningful work that helps improve
Responsibilities include, but are not limited to: • Trial and site administration: o Track (e.g. essential documents) and report o Ensure collation and distribution of study tools and documents • Document management: o Collate, distribute/ship, and archive clinical documents
Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guideline
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary: Support the setup, configuration, and
IQVIA Laboratories is a global leader in drug discovery and development laboratory services, offering a comprehensive suite of central laboratory and specialty biomarker services. Our expertise spans genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine a
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