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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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Mitarbeiter im Gesundheitswesen für die Abrechnungsprüfung (Bereich Pflege) (m/w/d) Wirke mit an der digitalen Transformation in der Gesundheitswirtschaft und profitiere von einer gesicherten wirtschaftlichen Perspektive. Neben anspruchsvollen und abwechslungsreichen Aufgaben mi
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Vue d’ensemble du poste Effectuer des tâches de suivi et de gestion de site pour une variété de protocoles, de sites et de domaines thérapeutiques. Doit être bilingue français et anglais et situé à Montréal. Responsabilités essentielles • Effectuer des visites de suivi des s
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Responsibilities • Carry out work relating to the HEOR business areas (e.g. database studies, longitudinal retrospective study using internal or external big data, longitudinal prospective observational study, cross-sectional survey of patients/healthcare provider/or payers, pat
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Associate Principal – Patient-Centered Solutions IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare informat
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Job Overview Under guidance, updates, and analyses data in the database to ensure it is correct. Provides systems support in developing and enhancing business systems to provide new or enhanced products to clients or effective planning, reporting, and analysis tools to internal f
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Job Title: Clinical Trial Nurse - Per Diem Work Set-Up: Local Travel – In patient Home Are you a Registered Nurse interested in Clinical Trial work? IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patient
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Job Overview Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Essential Functions • Actively prospect and leverage potential new business opportun
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Job Overview Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget. The Clinical Project Manager leads the regional clinical operations team (including oversight of external partners working on the regional leve
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JOB OVERVIEW Provide support and guidance to less experienced members of an HR team in their day-to-day operational roles. Support the continuous improvement of the HR function, through development and implementation for all HR programs in an assigned geography or assigned busi
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Join us on our exciting journey! We are recruiting a bold mind to work as a Senior Client Service Analyst with experience in client-facing roles, customer success, account management, or healthcare/pharmaceutical analytics. In this role, you will partner with leading pharmaceut
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Job Overview: The IT Internal Auditor position actively participates as a member of the audit team responsible for evaluating risks and controls within IQVIA’s business applications, IT infrastructure, and IT internal control environments with a focus on confidentiality, integri
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Job Overview Oversee a team of clinical database design professionals for delivery and build of multiple studies in various platforms. May act as a client contact from clinical database designing team & responsible for project financials, new scope of work, relationship developm
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About the Role Join IQVIA’s global Concierge Travel Services (ICTS) team, delivering a high-touch, “VIP” service for corporate travel and events. This role is responsible for managing complex global travel arrangements, designing seamless itineraries, and acting as a trusted adv
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Job Overview Provides leadership of the centralized monitoring team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract while opti
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Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. • A
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Job Overview Perform 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
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Job Overview Under moderate supervision, 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 manages site documentation; revi
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IQVIA Biotech is now hiring for CRA 2 with a minimum of 1.5 years of onsite monitoring, and early phase experience preferred. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned so
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Amphastar Pharmaceuticals, Inc. BAQSIMI® Job Description As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to the p
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Regulatory Affairs IVDR - Contractor (North Africa) Location: Algeria, Morocco, or Tunisia (Remote/Hybrid as applicable) Contract Type: Contractor About the Opportunity We are seeking an experienced Regulatory Affairs IVDR Contractor to support regulatory activities across the
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Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Sponsor Requirements: Prior experience in negotiat
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Job Responsibilities: Perform feasibility, site identification, site contract negotiation, and other study start-up activities, as assigned. Distribute and collect CDAs for potential study sites. Provide country-specific study start-up expertise to study start-up team leads an
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Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles,
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Job Overview Perform 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 v
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Join the Angels Initiative Team today! Every 30 minutes a stroke patient who could have been saved, dies or is permanently disabled, because they were treated in the wrong hospital. Our mission is simple. To increase the number of patients treated in stroke ready hospitals and