iqvia

IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solution

Attaché de recherche clinique II IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. Aperçu du poste L'ARC II est responsable de la surveillance des essais

Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable r

The Environmental, Health and Safety (EHS) Specialist will be responsible for the day-to-day implementation of site EHS policies and programs to provide a safe, healthy, and environmentally responsible workplace at the local level. This position is responsible for overseeing specific EHS programs ac

The Senior Supply Chain Coordinator's primary role is managing the Open Purchase Order and Cost Management. He/she is expected to support an average of ~400 unique Purchase Requests per month. The Senior Supply Chain Coordinator plays a critical role in supporting procurement operations. In addition

Job Overview Assists in maintaining and validating the project scope, plans and schedules for projects; adheres to established metrics for project success; applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance) Essential Functions • Assists in maintainin

Job Overview Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studi

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different t

Pharmacy Partnership Manager Patient Care & Education 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 verbete

Job OverviewUnder general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also in

El delegado se responsabilizará de la información y promoción de los productos de la Compañía en su zona geográfica de influencia, mejorando la experiencia del cliente, identificando necesidades críticas, y proporcionando soluciones óptimas para alcanzar los objetivos de negocio. Buscamos a profesio

Job Description Summary Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions• Perform site monitoring

Senior Site Activation Coordinator Location: FranceWork 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

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 Prepare documents and correspondence o Collate, distribute/ship, and archive clin

Description Job Overview:As a Recruiter you will play a crucial role in sourcing selecting and hiring qualified candidates to fill vacant positions within the organization. You will collaborate with management across various service areas business units or departments to ensure staffing objectives a

IQVIA™ is The Human Data Science Company™, combining data, technology, advanced analytics, and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem and drive meaningful progress in life science. JOB DES

◆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。 プロダクト戦略の立案から要件定義、開発推進、導入・定着化支援まで幅広く携わり、医療DXの実現に貢献できる環境です。将来的には、より大規模な事業開発や組織マネジメントを担っていただくことを期待しています。 ◆こんな方におすすめ！ ・医療情報システムの開発や導入経験を活かして社会

Job Description Summary Essential Functions• Monitors production environment using established tools and performs initial quality control for Italy Production Processes such as Dataview, SQL Analyzer, Sharepoint, Dashboard and Other third party tools• Execute production tasks, Quality audit, Data ma

Job OverviewProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinato

Job OverviewResponsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addit