Jobs at IQVIA

The Senior Clinical Research Associate will manage site monitoring visits, ensure compliance with GCP and ICH guidelines, and support project execution in clinical trials.

The Senior Scientist will lead biophysical characterization of antibodies, train team members, design assays, analyze data, and collaborate with teams to drive R&D efforts.

Lead product strategy, roadmap, and delivery for personalization and audience products that turn clinical and behavioral data into scalable, SaaS-based targeting and engagement solutions. Partner with engineering and data science to operationalize identity resolution, predictive models, and real-time triggers. Drive customer validation, go-to-market, and cross-functional alignment while ensuring privacy, compliance, and measurable client outcomes.

Monitor and validate incoming data for completeness and timeliness, investigate and resolve data queries with internal and external teams, run and manipulate database queries, implement quality control measures, and prepare requested reports. Provide systems support to enhance business reporting and analysis tools.

Support site-level clinical trial startup and administration: maintain TMF/eTMF and SharePoint uploads, coordinate EC submissions, process protocol amendments, update trackers, assist with contracts/payments, distribute site materials, and provide general administrative support.

Conduct site selection, initiation, monitoring, and close-out visits to ensure GCP/ICH compliance. Oversee enrollment, CRF completion, regulatory submissions, TMF/ISF document maintenance, site training, and cross-functional coordination to maintain data integrity and study progress.

作为研究中心团队成员，按照试验方案、GCP及SOP协调并执行临床试验：支持可行性评估、中心启动、受试者筛选入组、随访与药物/样本管理，进行CRF数据录入与query处理，参与监查/稽查/会议，推动中心关闭并维护工作报告。可能需不定时出差或借调。

Drive new and retained clinical sponsor business through consultative sales: prospect accounts, build relationships with decision-makers, propose solutions, coordinate proposals/contracts, lead sales presentations, record CRM activity, and ensure customer satisfaction while meeting financial targets.

Support IVDR transition projects and regulatory submissions for IVD products across EMEA. Coordinate change control, product registrations, and regulatory dossiers with cross-functional teams, maintain regulatory databases, monitor legislation, assess regulatory impacts, track milestones, and provide local Regulatory Affairs backup and stakeholder representation for compliance activities.

Lead end-to-end implementations of Hospital Information Systems and Revenue Cycle Management: plan, design, build, test, deploy, and support go-live. Manage timelines, stakeholders, cross-functional teams, risk mitigation, change management, user adoption, and post-go-live stabilization while ensuring alignment with clinical workflows and revenue cycle processes.

Perform site monitoring and management to ensure protocol compliance, data integrity, and regulatory adherence (GCP/ICH). Conduct site selection, initiation, monitoring and close-out visits; train and communicate with sites; track regulatory submissions, recruitment, CRF completion, and TMF/ISF documentation; generate visit reports and action plans; liaise with study teams and may support recruitment planning and site financial management.

Develop, optimize, validate, and transfer flow cytometry assays and methods. Lead low-to-moderately complex technical projects, troubleshoot and optimize processes, support analytical testing delivery, collaborate cross-functionally, and mentor junior staff while contributing to reports and scientific communications.

Maintain and update complex pharmaceutical reference data (pharmacy, hospital, outlet, NDF, TAPS, OneKey) for AU/NZ production; perform geocoding in MapInfo; verify data by phone and email; bridge incoming transaction data to reference files; liaise with suppliers and internal teams to ensure data accuracy and timeliness.

Senior, client-facing leader responsible for end-to-end MedTech market research and consulting engagements. Leads study design, synthesis of qualitative and quantitative insights, presents to senior stakeholders, owns project delivery and revenue targets, mentors teams, and drives business development and thought leadership across global accounts.

Lead and manage QA oversight for projects and staff, plan and conduct GxP/GCP audits and inspections, investigate quality issues, provide regulatory consultation and training, maintain eQMS metrics and SOPs, and serve as QA liaison to internal and external stakeholders.

Lead regional clinical operations for assigned studies from feasibility through closeout. Manage regional teams and vendors, ensure regulatory submissions, inspection readiness, TMF quality, site monitoring oversight, timelines, budgets, and cross-functional alignment with global study objectives.

Lead design and development of scalable, high-performance cloud-native healthcare systems for payer and provider use cases. Build claims adjudication and payment platforms, design APIs and interoperability, drive architecture and engineering standards, mentor teams, implement CI/CD and DevOps practices, and optimize systems for high-volume claims processing while ensuring compliance and collaboration with product and clinical stakeholders.

Support Transparency reporting for Compliance Services: validate and remediate data, perform analytics, generate and articulate draft reports, request and track client information, conduct quality reviews, automate reporting with BI tools, and provide weekly status updates to stakeholders.

Deliver strategic consulting and analytic support to life sciences clients: research, quantitative and qualitative analysis, client-facing presentations, project management, and team leadership to develop commercial solutions and recommendations.

Provide regulatory oversight for clinical trial submissions across EMEA/global programs: prepare and review regulatory documents (e.g., IMPDs), manage centralized and country submissions, ensure compliance and timely deliverables, support stakeholders and business development, deliver training, maintain records, and mentor junior staff.