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Job Overview Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales process. • Participates or leads teams in the d
Job Overview IQVIA is looking for an experienced Clinical Coding Auditor to join our team based in London, UK. NHS Approved/Accredited Clinical Coding Auditor responsible for: • Producing monthly data quality and targeted audit reports • Delivering clinical coding audits, inclu
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 deliv
IQVIA Discovery Sciences is seeking an experienced, innovative, and highly motivated Scientist to join our Analytical and Purification Sciences team at our Cambridge site. This is an exciting opportunity to work within a collaborative, multidisciplinary environment, where you wi
IQVIA's PPG Provider team helps health systems grow by combining industry expertise, data, technology, and marketing solutions that strengthen patient acquisition, physician engagement, brand performance, and service line growth. The Associate Director, Sales is responsible for
Job Overview The Clinical Functional Service Partnerships (CFSP) Project Team are responsible for the management of multiple global projects for assigned clients and serve as key operational finance contact points. The team is also involved in supporting the strategic decisions
We are hiring multiple headcounts for our Flow Cytometry team, which requires working on shifts: either a Tue-Sat or Sun-Thu workweek. Please apply only if you are comfortable. - Responsible for performing and documenting analytical procedures in accordance with SOPs and regulat
Job Overview Provide 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
- Maintains the QA database(s) ensuring Audits when identified are entered onto the system from audit plans/notification documentation and that the system is updated as required. - Audit information is followed up as required, through the full audit life cycle including: Missing
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. - Career development opportunities to grow as we grow - Flexible working to assist work–life balan
Job Overview Clinical Research Associate performs monitoring and site management work to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. - Perform site monit
Clinical Project Managers 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 Clinical Project Manager is an essential member of the core project team responsible for project deli
We are seeking Associate Scientist to join IQVIA Laboratories at Valencia, CA. 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
Contract Remote Role – Location (Open to Remote US) At IQVIA, we are driven by a shared purpose: to improve patients’ lives through innovative healthcare solutions. As a global leader in commercial services, we bring life-changing therapies and support programs to the people who
Job Overview The Site Strategy Lead (SSL) is integral to the development of our delivery strategies at the very early phase of proposal development, and is a key player in supporting the study specific requests for the Data Generation group from the clients in the request for pr
- 1年以上CRC/CTA/SSU工作经验; - 5个月以上CRA经验; - - 薪酬福利:具有市场竞争力的薪资,完善的福利体系 - 完善保障:五险一金 + 补充商业医疗保险 - 休假权益:充足的带薪年假与病假,工作生活更平衡 - 成长空间:清晰的职业发展路径,助你稳步晋升 - 强大支持:全球领先药企与IQVIA的培训体系,资源与平台双重加持
We are seeking Operational Quality Specialist to join IQVIA Laboratories at Buenos Aires, Argentina. 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 tr
Sponsor dedicated - 100% Home based role. Job Overview The Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in R and SAS programming and familiari
Our MedTech Depot Field Service Technician experiences a unique opportunity to utilize their previous work roles in an effort to advance their careers into the medical device industry. This position is 40 hours per week. What you will be doing in the role: - Receives incoming d
Job Overview - Ensures that the quality of task completion is acceptable and accurate by reviewing the daily work produced by the team. - Ensures that the work is meeting the required specifications/procedures and requirements through daily audits. - Responsible for auditing qu
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