Jobs at IQVIA

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

Perform QA testing for complex pharmacy-related software: write test plans and scripts, execute tests, document and resolve defects, validate backend databases, recommend process improvements, and establish software quality standards.

The Consultant will manage and lead multiple consulting engagements, deliver strategic insights, and build trusted client relationships in the healthcare sector.

As a Sr Principal, you will develop client relationships, drive business development opportunities, lead projects, and mentor team members within the life sciences sector, focusing on collaborative problem-solving and client satisfaction.

This role involves business development, client relationship management, project leadership, and team development in the life sciences consulting domain, focusing on delivering custom solutions for clients.

This role drives sales by developing strategies, generating business leads, managing client engagements, negotiating contracts, and collaborating with internal teams to enhance market presence and client satisfaction.

This role focuses on selling a portfolio of solutions in life's science, managing sales, developing tailored solutions, and achieving revenue targets.

Senior lead driving Technology & AI strategy, solution architecture, and delivery for biopharma commercial analytics. Responsibilities include client-facing business development, practice building, embedding GenAI/ML and cloud data platforms, architecting scalable data/AI solutions, and publishing thought leadership.

Lead and execute site monitoring visits per GCP/ICH, build site relationships, ensure protocol compliance and data integrity, track study progress and regulatory approvals, identify and escalate risks, maintain documentation and inspection readiness, and collaborate with cross-functional teams to deliver high-quality clinical trials.

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.

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.

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

Lead global client relationships for a large pharma account, define and execute commercial and medical affairs asset strategies, drive revenue growth, orchestrate cross-functional IQVIA teams, influence senior stakeholders, and sell large-scale integrated solutions across Consulting, Analytics, RWE, and Medical Affairs.

Lead end-to-end global clinical study site management for oncology Phase I-III trials. Own site selection, activation, monitoring oversight, risk mitigation, financials, TMF health, and client/stakeholder engagement while ensuring ICH-GCP and regulatory compliance.

Manage multiple consulting projects for pharmaceutical clients, ensuring timely and budget-conscious deliveries while providing strategic direction and client support.

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