iqvia

IQVIA is looking to recruit a new CPM/Senior Clinical Project Managers (Sr CPM) to work as an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. This position will be an essential member of the core project team leading the team and responsible for project delivery...

Our ever-growing Lifecycle Safety Medical team is expanding. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios,...

IRT Systems Project Manager We are seeking an experienced IRT Systems Project Manager to lead the design, implementation, and delivery of Interactive Response Technology (IRT) solutions supporting global clinical trials. In this highly consultative role, you will partner with pharmaceutical and biotechnology clients to translate complex clinical study...

Job Overview With applicable guidance, responsible for remote site monitoring activities to ensure sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. May monitor and/or co-monitor on-site when needed. May perform Site Identification (Site ID) and/or...

The Qualified Person Responsible for Pharmacovigilance (QPPV) is a mandatory position Marketing Authorization Holders (MAHs) are required to have when operating as entities in the European Union (EU). The QPPV is responsible for the establishment and maintenance of the MAH’s pharmacovigilance system.The Associate Marketed Product Safety director  is...

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department. In this role, you 'll become an expert in Vendor Management...

Europe-based | Business Development | Life Sciences & Healthcare The opportunity IQVIA Language Solutions is building the multilingual operating layer for global life sciences—bringing together healthcare intelligence, AI-enabled workflows, specialist human expertise and the reach of IQVIA. We are moving beyond traditional translation to help customers...

Senior Site Activation CoordinatorLocation: Romania (Hybrid)Job Type: Full-timeJoin IQVIA and Help Advance Clinical ResearchIQVIA is seeking a Site Activation Specialist to support clinical research studies across Romania. In this role, you will be responsible for executing site activation, regulatory, and start-up activities while working closely with...

At IQVIA, we are committed to advancing healthcare through innovative clinical research. We are currently seeking an experienced Clinical Trials Assistant to join our Sponsor-Dedicated Functional Service Provider (FSP) team in Romania.In this role, you will provide essential support to project teams in the successful execution of clinical trials across a...

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 visits (selection, initiation, monitoring and close-out visits) in accordance with...

Senior Site Activation Coordinator Location: Romania (Hybrid) Job Type: Full-time Join IQVIA and Help Advance Clinical Research IQVIA is seeking a Site Activation Specialist to support clinical research studies across Romania. In this role, you will be responsible for executing site activation, regulatory, and start-up activities while working closely with...

At IQVIA, we are committed to advancing healthcare through innovative clinical research. We are currently seeking a Senior Clinical Trials Assistant to join our Sponsor-Dedicated Functional Service Provider (FSP) team in Romania. In this role, you will provide essential support to project teams in the successful execution of clinical trials across a variety...

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 visits (selection, initiation, monitoring and close-out visits) in accordance...

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 experienced Regulatory Affairs professional with significant expertise in Advertising &...

At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and accelerate access to innovative therapies. We are seeking an experienced Regulatory Affairs professional with deep expertise in European regulatory affairs and biologic products. This role is ideal...

Clinical Operations Intern | RomaniaAbout the RoleAs a Clinical Operations Intern, you will gain hands-on experience supporting reporting, analytics, and operational activities within a dynamic clinical research environment. This internship offers an excellent opportunity to develop analytical skills, work with industry-leading reporting tools, and...

PURPOSE Provide administrative support to clinical projects under direction of line manager, Clinical Research Specialist and/or other designated clinical team members. Assists with general administrative functions as required.RESPONSIBILITIES · Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research...

At IQVIA, we advance healthcare by providing scientific solutions that span clinical trials, real-world evidence, and consulting services across the entire product lifecycle. Our Instrument Licensing Services team manages and licenses a diverse portfolio of Clinical Outcome Assessments (COAs), supporting their implementation, translation, scoring, and use...

PURPOSE Provide administrative support to clinical projects under direction of line manager, Clinical Research Specialist and/or other designated clinical team members. Assists with general administrative functions as required. Responsibilities • Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research...

Clinical Operations Intern | Romania About the Role As a Clinical Operations Intern, you will gain hands-on experience supporting reporting, analytics, and operational activities within a dynamic clinical research environment. This internship offers an excellent opportunity to develop analytical skills, work with industry-leading reporting tools, and...