Jobs at IQVIA

Design, develop, and maintain scalable React-based web applications, contributing to front-end and back-end development, APIs, integrations, testing, documentation, and production support. Translate business needs into technical solutions, improve application performance and reliability, and mentor junior developers. Collaborate with cross-functional teams across Canada and internationally while promoting engineering best practices, CI/CD, automated testing, and code quality.

Leads scientific and pharmaceutical pricing assessments, literature reviews, PMPRB submissions, client recommendations, presentations, and regulatory deliverables. Manages concurrent client projects, timelines, resources, budgets, and risks while maintaining quality standards. Serves as a client-facing project lead, interprets pricing policies, mentors junior staff, reviews scientific work, and contributes to process improvement, proposals, and business growth.

Leads global governance and operational oversight for a pharmaceutical customer’s portfolio of product development projects. Responsibilities include strategic account management, operational standards, contractual and financial performance, resource forecasting, client relationship management, escalation planning, governance committees, sales support, and adherence to IQVIA best practices. Requires extensive pharmaceutical or CRO industry experience, strong leadership, negotiation, communication, and decision-making skills, and up to 25% travel.

Provides Tier 2 technical and operational support for Veeva CRM, Vault, Network, and Vault CRM. Responsibilities include resolving escalated incidents and service requests, performing root-cause analysis, managing configurations and environments, monitoring performance, documenting solutions, coordinating with teams and vendors, and maintaining client relationships. Requires Veeva CRM experience and certification, knowledge of pharmaceutical sales processes, data migration, compliance, and ticketing systems. Vault and Network experience or certification is preferred.

Lead execution of global oncology clinical trials ensuring ICH/GCP compliance, meeting recruitment targets, managing clinical risk and EAC budgets, assuring quality, coordinating stakeholders, coaching clinical teams, supporting proposals, and mentoring staff as needed.

Manage a portfolio of pharmaceutical clients using consultative selling to drive revenue for reimbursement and patient support solutions. Develop strategic account plans, lead cross-functional teams, manage program renewals, and maintain accurate pipeline forecasting to meet growth targets and ensure high client satisfaction.

Supports life sciences consulting projects focused on oncology by analyzing client needs, conducting interviews with oncologists and payers, working with registry and claims/LRx datasets, developing documentation and presentations, and translating quantitative and qualitative findings into actionable recommendations. The role operates under close supervision, builds consulting and oncology market expertise, collaborates across teams, and frequently participates in client presentations requiring travel.

Manage end-to-end client-specific patient support programs: set up, launch, monitor performance, escalate risks, produce client reports, and lead a team of caseworkers ensuring QA, KPIs, SOP compliance, and continuous improvement.

Lead client relationships and oversee operational and financial portfolio for connected devices in clinical research. Support department strategy, ensure FDA/ICH GCP compliance, manage SOPs and quality control, conduct capacity planning, assist RFP/RFI responses, oversee forecasting and backlog, mentor new hires, and drive process improvement initiatives to ensure high-quality delivery.

The Associate Consultant will provide analytical support for client projects in life sciences, assist in developing proposals, conduct quantitative analyses, and communicate findings to stakeholders, while working collaboratively in a team environment.

Provide high-quality analytical support to life sciences client projects: perform quantitative and qualitative analyses, develop client deliverables (Excel/Power BI/PowerPoint), own defined workstreams, support client interactions, and contribute to internal knowledge and tool development. Work with imperfect data, document assumptions, and collaborate with senior consultants to deliver timely recommendations.

The Senior Clinical Research Associate is responsible for site management, monitoring visits, training staff, and ensuring compliance with regulatory requirements in clinical research.