Jobs at IQVIA

The CRA 2 will conduct site monitoring visits, manage studies, ensure regulatory compliance, and support recruitment strategies in oncology.

Lead and oversee operational aspects of Linguistic Validation and eCOA projects: create and track timelines, manage budgets and invoicing, report status and financials, coordinate cross-functional teams, ensure SOP compliance, mentor junior PMs, support proposals, and drive process improvements to meet quality and timeline metrics.

Lead design and optimization of large-scale data pipelines and workflows for forecasting and analytics. Work across backend stack, ensure code quality, collaborate with product and engineering teams, mentor junior engineers, and translate business requirements into scalable cloud-based data solutions.

Lead national payer account management and market access activities for pharmaceutical/biotech clients. Manage and coach National Account Directors, develop managed care strategies, track performance, support client presentations, and monitor team workloads. Ensure formulary coverage goals are met and provide strategic recommendations to clients and IQVIA leadership.

The Clinical Research Associate will conduct monitoring visits, ensure compliance with study protocols, manage site communications, and support regulatory submissions and study management.

The CRA I supports clinical research by monitoring sites, ensuring compliance with regulations, and maintaining communication with investigative sites. Responsibilities include site visits, protocol training, and documentation preparation.

The Business Development Director secures and retains business through proactive sales, cultivates relationships, analyzes opportunities, coordinates sales teams, and monitors customer satisfaction.

Drive volume and market-share growth for assigned pharmaceutical GI products within a territory by building relationships with healthcare providers, delivering sales presentations, managing samples and promotional materials per FDA/PDMA guidelines, documenting activity in the sales automation system, and completing required product training.

Lead end-to-end development, validation, and operationalization of connected medical device and digital health solutions for respiratory trials. Partner with strategy to evaluate solutions, own startup execution from approval through Business Go‑Live, coordinate cross-functional teams (Engineering, QA, Regulatory, Data, Operations, vendors), ensure readiness, quality, and compliance, manage risks/escalations, and support commercialization and stakeholder communications for scalable study deployment.

Lead national Community Medical Liaison program for Johnson & Johnson Neuroscience. Provide strategic project leadership, client relationship management, cross-functional planning, team development, operational oversight, compliance, field coaching, performance tracking, and program enhancements to meet contractual and clinical education objectives.

Lead vision, strategy, and roadmap for Media OS, evolving it into an AI-powered, privacy-first healthcare marketing platform. Drive product, partnerships, and go-to-market plans across audience, identity, activation, measurement, and integrations to increase adoption, revenue, and campaign performance while managing cross-functional teams and stakeholders.

Identify and close new business opportunities selling registry technology, clinical decision support, and value-based care solutions to medical specialty societies. Manage full sales cycle, build pipelines, develop proposals, negotiate contracts, track activity in CRM, and collaborate with internal technical and operational teams to deliver solutions and meet quota.

Manage client relationships for mid-sized clients, assist in selling services, identify expansion opportunities, and ensure customer satisfaction.

Manage medium-to-large multi-regional connected devices projects across all clinical trial phases. Plan, execute, and deliver projects to scope, schedule, and budget; lead cross-functional teams; track risks and finances; ensure SOP-compliant deliverables; communicate with sponsors; prepare reports; conduct project closeouts; and mentor junior project managers.

Promote endocrinology/diabetes products via phone to healthcare professionals, achieve sales forecasts, build relationships with targeted accounts and physicians, coordinate sales strategies with teammates, handle CRM and multi-task in real-time, accept coaching, and provide accurate product information to drive adoption and utilization.

Lead and manage strategic, operational, and financial site activation activities across multiple regions. Oversee site identification, regulatory submissions, contract negotiation, project plans, and compliance with ICH-GCP. Provide regulatory intelligence, stakeholder communication, reporting, mentoring, and support pre-award/bid activities to accelerate site start-up and patient enrollment.

Field-based pharmaceutical sales role driving volume and market share for GI products in an assigned territory. Build relationships with physicians and HCPs, deliver sales presentations, manage samples and promotional materials per FDA/PDMA guidelines, document activity in the sales automation system, and complete required product training.

Make outbound calls to optometrists and ophthalmologists to discuss presbyopia clinical information, record activities in CRM, meet productivity targets, handle inbound calls as needed, coordinate with teammates, participate in training and events, and maintain up-to-date market and HCP records.

Responsible for leading site monitoring visits, ensuring protocol compliance and data integrity, while collaborating with teams for effective study execution.

The Clinical Research Associate will lead site monitoring visits, ensuring compliance and data integrity while managing study progress and regulatory approvals.