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Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
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To be eligible for this position, you must reside in the same country/sales region where the job is located. Position Summary The Associate Business Development Director - Clinical Technology Sales is responsible for driving revenue growth across IQVIA’s Clinical Technologies p
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Territory Area: Wales Do you want to join a company that nurtures its employees and advocates for an employee work-life balance? Do you have excellent sales experience and wish to join a company that has led the way in the development, manufacture, and marketing of innovative de
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Location: Southeast London / Southwest London Are you hungry to make your mark in oncology? This is a rare opportunity to step into a high‑impact oncology role, working with respected, life‑changing products that sit at the heart of patient care. We are looking for someone d
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Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Proce
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IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing
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IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing
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We are seeking an Associate Manager, Flow Cytometry to join IQVIA Laboratories on site at Valencia. 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 tra
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IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing
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Ervaring als medisch afgevaardigde op zak en zin om verder te bouwen? In deze rol krijg je autonomie en de kans om je talenten volop te ontwikkelen in het veld. Wat houdt de job in? Promotie van het Sandoz‑portfolio bij huisartsen, specialisten en apothekers. Analyseren van ma
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Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include ma
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Under moderate supervision, the Regulatory and Start Up Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manage
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Role Purpose: Responsible for the daily maintenance of healthcare Organizations and Prescribers in all database of the US Region. Validates, research & analyses to client data inquiries with the use of the process tool. Job Responsibilities: Complete maintenance of reference
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Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOP
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Job Description Summary: Under appropriate guidance, ensure that personal administration and HR processes are executed in-country in full compliance with local labor legislation, Core HR standards, and corporate policies. The role is offered as a two-year maternity cover. Core
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V Voor een opportuniteit bij één van onze klanten zoekt IQVIA een ervaren, gedreven farmaceutisch afgevaardigde. Je komt terecht bij een internationale farmaceutische speler , actief in de ontwikkeling en commercialisering van kwalitatieve geneesmiddelen. Wat houdt de job in?
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담당 업무 및 자격 요건 • 3년 이상의 마케터 경험 • 헬스케어 메디컬 마케팅 프로젝트 기획 / 운영 및 고객사 커뮤니케이션 [Medical Contents] - Slide : Master Slide Deck 구성, Detail Slide 기획 - Materials : 제약 마케팅 머터리얼 기획 (브로셔, 리플렛, 카드 뉴스 등) - Detail Kits : 의사/환자 대상 안내 책자 키트 기획 - Motion Graphic (including Film) : 브랜드 영상 기획 (2D 인포그래
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Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include ma
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Overview: Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation
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Job Overview Develop and prepare contracts and budgets for assigned customers, to support the global sales team. Essential Functions • Work closely with project teams to determine appropriate terms and conditions of contracts under supervision. Alternatively, be involved in prep
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Systems Design Project Manager – IRT Basil, Switzerland About the Role The Systems Design Project Manager (IRT) plays a key role in supporting clinical trials by designing and delivering IRT systems that ensure patients receive the correct study drug according to protocol. Yo
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Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role acts as a strategic partner to both external and internal stakeholders to optimize the site experience and pe
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Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance act
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Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role acts as a strategic partner to both external and internal stakeholders to optimize the site experience and pe
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Please note that fluency in German language is an absolute must for this role. About IQVIA: IQVIA is a fast-growing and highly successful business, delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem. Leveraging access to
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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