Jobs at IQVIA

Oversee site monitoring and management, ensure compliance with protocols, and facilitate recruitment and training for clinical studies.

Responsible for site monitoring and management in oncology clinical trials, ensuring compliance with protocols and regulations while managing site relationships and documentation.

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

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

Lead global engineering managers and senior engineers to own architecture, delivery, and operations for API and data platforms. Define technology strategy, ensure scalable data pipelines and integrations, enforce SDLC and operational excellence, manage budgets and vendors, and develop engineering leadership and succession plans.

Lead and build the ATS Sales Enablement function, translating product capabilities into value-based sales motions and enablement assets. Partner cross-functionally with Product, Marketing, Sales, Pricing, and RevOps to support launches, create content, and measure enablement impact on pipeline and sales effectiveness.

Lead data management for complex global clinical trials, ensuring quality and compliance while mentoring staff and driving process improvements.

Perform national onsite quality and regulatory inspections across up to three locations weekly. Maintain documentation in a heavily regulated environment, work with minimal supervision on flexible schedules, meet hospital vendor credentialing, and support validation, auditing, and client-facing quality activities. Travel and 40-hour availability required.

Promote a GI-focused therapeutic via inbound/outbound outreach, achieve sales quota, build physician and account relationships, coordinate sales strategies, maintain CRM records, complete product training, and ensure compliance with promotional programs and reporting.

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

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.

Provide remote and on-site technical support for automated medication dispensing systems: install software patches, troubleshoot hardware/software/networking, document service actions, escalate complex issues, obtain vendor and hospital credentialing, and perform physical tasks up to 70 lbs. Part-time, as-needed schedule with potential travel to customer sites.

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

As a Product Manager, lead the design and optimization of data pipelines, ensuring scalability and performance in healthcare data solutions, while supporting AI initiatives and collaborating with cross-functional teams.

The Principal Enterprise Architect leads architecture for M&A initiatives, defining strategies for rapid integrations, assessing technology landscapes, and mentoring senior architects.

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.

The CRA will lead site monitoring visits, ensure compliance with protocols, build relationships with sites, and manage study progress.

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.