Recibir nuevas ofertas de empleo por email
- ...delivery across diverse therapeutic areas. The role involves managing study quality, patient recruitment, site performance, and cross-... ...Responsibilities Lead clinical delivery of regional and global studies, ensuring quality, timeline, and recruitment targets Drive...
- ...enrollment, drive regulatory submissions, and ensure successful study execution across diverse therapeutic areas. Responsibilities... ...managing study timelines, risks, quality, budgets across complex studies ~ Demonstrated stakeholder management and relationship-building...
- ...IQVIA seeks a Global Study Associate Director to lead clinical study delivery across multiple sites in Latin America. This role oversees cross-functional teams, manages study timelines and budgets, ensures regulatory compliance, and serves as the primary liaison between...
- ...Reporting to the Team Lead, Deal Desk, the Deal Support Coordinator role focuses on transactional deal support and administrative tasks that help our sales team close business efficiently. If you enjoy data accuracy, policy and process, working with systems, and supporting...
- ...IQVIA seeks a Site Activation Coordinator to support feasibility assessments and site initiation activities for clinical research studies across North America. The role involves managing site documentation, tracking regulatory submissions, and serving as primary contact...
- ...Maintenance Associate role supporting the delivery of clinical studies during their maintenance phase. The position involves coordinating with cross-functional teams to ensure timely completion of regulatory activities, system management, and compliance tracking across...
- ...reviewing structured data outputs, identifying anomalies, and coordinating with clinical sites and internal teams. Responsibilities... ...medical history completeness Verify end-of-treatment and end-of-study documentation accuracy Collaborate with medical review...
- ...across Argentina, Mexico, and Brazil. The role involves managing documentation, system access, training coordination, and meeting logistics to ensure timely study delivery and regulatory compliance. Responsibilities Coordinate system access and permissions for project...
- ...expectations for requirements quality and traceability, advise on novel study designs, and resolve critical requirements issues across... ...for technical execution and evidence while supporting overall coordination by the Lead Data Manager. - Production Readiness, Migration,...
- ...site agreements. The role involves managing contract templates, coordinating translations, reviewing budgets, and liaising with sponsors,... ...clinical sites Coordinate document translations and review study budgets for cost and compliance Escalate requests outside approved...
- ...as global medical advisor on assigned clinical trials Review protocols, investigator brochures, case report forms, and clinical study reports Provide medical support to investigative sites on protocol issues and patient safety Assess and clarify adverse events...
- ...IQVIA seeks a senior site activation specialist based in Argentina or Brazil to coordinate clinical trial site preparation activities across North American studies. The role involves managing documentation, regulatory compliance, and communication between investigative...
- ...protocols, safety data, adverse events, and critical clinical findings; ensure GCP compliance and timely safety reporting Train study teams and investigators on protocol and therapeutic area; support site selection and patient recruitment strategies Review clinical...
- ...regulatory submissions, contracting, and essential document processes Develop and execute Site Activation Management Plans aligned with study strategy and timelines Collaborate with internal teams and external stakeholders to ensure efficient study start-up execution...
- ...Write code, perform testing, debugging, and documentation of applications using current programming languages Prepare feasibility studies and system test data for new and revised programs Complete installation and maintenance procedures and documentation...
- ...Clinical Operations, and Regulatory Affairs. Translate clinical and scientific requirements into scalable technical solutions that support study execution and data delivery. Database Design & Optimization: Lead the design and optimization of secure, high-performance relational...
- ...The role involves managing site feasibility, regulatory documentation, contracting, and performance tracking for clinical research studies, working closely with project teams and investigative sites. Responsibilities Serve as primary contact for site feasibility,...
- ...activities and facilitate quality decision-making across clinical programs Identify, assess, and mitigate quality risks throughout study execution Analyze quality metrics and trends to drive proactive improvements and performance enhancement Requirements...
- ...integral part in the overall success of our account team’s delivery and service to our clients, serving as the communications and coordinating hub between team members and the client. This role will report directly into the Client Experience team,, and will be supported...