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- ...Lead global site activation strategies across multiple regions to accelerate clinical trial enrollment. Manage site identification, regulatory submissions, contracting, and lifecycle operations while ensuring compliance with ICH-GCP standards and project timelines....
- ...time. They are actively involved in supporting reporting, optimizations, and routine campaign management. They are a self-starter when it comes to their responsibilities and manage their workflow efficiently and effectively. ***Proficiency in spoken and written English at...
- ...IQVIA seeks a Medical Data Review Manager specializing in rheumatology to evaluate clinical trial patient data for medical plausibility, protocol adherence, and completeness. The home-based, global position requires reviewing structured data outputs, identifying anomalies...
- ...Proficiency in spoken and written English at an advanced level is required for this role. A day in the life: The Digital Marketing Project Manager will play an integral part in the overall success of our account team’s delivery and service to our clients, serving as the...
- ...IQVIA seeks an Associate Site Activation Manager to lead global clinical trial start-up and site activation activities across multiple regions. The role involves partnering with sponsors and investigative sites to accelerate patient enrollment, drive regulatory submissions...
- ...teams to ensure timely completion of regulatory activities, system management, and compliance tracking across assigned studies.... ...interpersonal, communication, and organizational abilities Ability to manage multiple concurrent projects Capacity to work across different...
- ...day in the life: As a Systems Administrator, you keep Power Digital's core platforms running and well-governed. Reporting to the Sr. Manager, IT, you are the hands-on administrator for Google Workspace, Okta and Slack, and you support Power Digital's (PDM) internal...
- ...study physician or in pharma, CRO, biotech ~ Advanced English proficiency; fluent communication with diverse stakeholders ~ Strong collaboration and independent project management skills ~ Ability to translate complex medical concepts into actionable insights...
- ...Google Workspace, Microsoft Suite and Adobe tools a plus. - Strong attention to detail, accuracy, and consistency in work. - Ability to manage multiple tasks and meet deadlines in a fast-paced environment. - Strong communicator in English at a professional level (written...
- ...service within the broader media mix. You are responsible for owning reporting, optimizations, client communication, and execution of keyword research, ad copy development, bid optimizations, and routine campaign management, sometimes with the support of a Specialist....
- ..., ad copy development, bid optimizations, and routine campaign management, sometimes with the support of a Specialist. The Strategist is... ...optimizations with regard to performance improvements relative to goals - Manage all client budgets and/or advise on budget changes based on...
- ...trial delivery across diverse therapeutic areas. The role involves managing study quality, patient recruitment, site performance, and cross... ...and teams to advance study milestones and resolve issues Manage clinical risks, oversee quality standards, and implement...
- ...teams across Argentina, Mexico, and Brazil. The role involves managing documentation, system access, training coordination, and meeting... ...Strong organizational and attention-to-detail skills Ability to manage multiple priorities independently and collaboratively...
- ...in the life: As the Director of Paid Advertising, you are the leader of your pod, a hybrid of senior individual contributor, people manager, and product leader for your channel of expertise (Creative, Paid Media, Organic Search, or Social) within the division. Reporting...
- ...complexity out of the financial workflows–including everything from global payments and compliance to multi-currency and workforce management, to providing working capital and business intelligence–we give businesses the tools they need to work efficiently worldwide and...
- ...We’re expanding our data management capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru , and we’re hiring a Senior... ...while supporting overall coordination by the Lead Data Manager. - Production Readiness, Migration, Change Control & Archival:...
- ...conversations as the subject-matter expert, guide a growing team of Media Managers, and confidently recommend (and defend) strategies that drive... ..., road-mapping, testing frameworks, and campaign ideation. - Manage and mentor a team of 1–2+ Media Managers, supporting their...
- ...escalation - Leverage the Nova ecosystem, AI technologies, and Power Digital workflows (Asana, Slack, novaPulse, Google Drive) to manage workflow and support execution - Power Circuit completion and adoption across all assigned accounts - Adoption and completion of Omega...
- ...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 study teams and clinical...
- ...scalable validation frameworks that proactively detect and resolve systemic data issues. Serve as a strategic partner to Clinical Data Managers and cross-functional teams, driving continuous improvement in data integrity across global trials Programming & Scripting:...
- ...Contracts Specialist for Buenos Aires and Brasilia to develop, negotiate, and finalize clinical trial site agreements. The role involves managing contract templates, coordinating translations, reviewing budgets, and liaising with sponsors, sites, and internal teams throughout...
- ...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 between investigative sites and internal teams...
- ...North America team based in Argentina or Brazil. The role involves managing site feasibility, regulatory documentation, contracting, and... ...activities across assigned studies Prepare, review, and manage site documentation including regulatory, contractual, and ethics...
- ...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 sites and internal teams. Responsibilities Serve...
- ...involves strategic quality governance, regulatory compliance, risk management, and inspection readiness across clinical research programs... ...sciences organizations Proven ability to assess quality risks and manage complex quality issues Experience with audits, inspections,...
- ...applying appropriate evaluation practices to LLM-powered and AI-assisted functionality.. - Partner closely with Engineering, Product Management, and Product Design to refine ambiguous work into clearly defined, valuable deliverables.. - Maintain reliable systems by...