Jobs at IQVIA

Lead strategic, operational and financial delivery of site activation for clinical studies, including site identification/selection, ethics and regulatory submissions, contracting, project planning, stakeholder coordination, reporting, and mentoring to accelerate site start-up and maintain study approvals in compliance with ICH-GCP and sponsor requirements.

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.

Lead clinical delivery for multi-regional trials, manage clinical teams, recruitment, risk mitigation, clinical quality and project finances (EAC). Liaise with stakeholders, support resourcing and talent development, contribute to proposal strategy and may perform site visits.

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.

Conducts monitoring visits for Phase I-IV oncology clinical trials, ensuring protocol, GCP/ICH, and regulatory compliance. Trains site personnel, verifies source documentation and data integrity, resolves queries, oversees investigational product accountability and regulatory documents, maintains site communications, prepares monitoring reports, and supports investigator meetings. This home-based Eastern Canada role requires French-English bilingual fluency and 65-70% travel.

Plans, conducts, documents, and closes independent pharmaceutical quality audits across applicable countries. Evaluates findings, advises teams and clients on regulatory compliance, manages quality issues, reviews RCA and CAPA plans, supports inspections, maintains eQMS audit records, delivers training, and leads quality assurance improvement initiatives and consulting projects.

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.

Manage assigned clinical studies from initiation through closeout, performing centralized and remote monitoring, subject-level data review, risk-based monitoring, trend analysis, and site oversight. Ensure data integrity, participant safety, regulatory and ICH-GCP compliance, prepare i-Site packs and reports, mentor junior monitors, support project teams, and maintain audit-ready documentation and clinical systems.

The Clinical Research Associate II is responsible for monitoring oncology clinical trials, ensuring compliance, training site personnel, conducting visits, and managing documentation.

Lead and deliver medium-to-large multi-regional oncology clinical trials. Develop study strategy and integrated management plans, manage cross-functional teams, clients, risks, regulatory compliance (ICH GCP), and project financials. Mentor staff and drive operational excellence, quality, and timely milestones.

The Senior Clinical Research Associate oversees site management and monitoring activities for clinical trials, ensuring regulatory compliance and effective communication with sites to achieve project goals.

Perform monitoring and site management to ensure compliance with study protocols, regulations, and sponsor requirements, including site visits and documentation.

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 monitoring site activities, managing clinical trials, ensuring compliance with regulations, and mentoring clinical staff.

Provides bilingual telephone, email, and web-based support for pharmaceutical patient assistance programs. Responsibilities include clinical and treatment support, patient counseling, adherence assistance, adverse-event reporting, reimbursement and insurance navigation, financial assessments, special authorization and appeals support, copay and bridging arrangements, case review, and coordination with patients, healthcare professionals, insurers, and pharmaceutical manufacturers.

Supports the lifecycle management, commercialization, licensing, and client delivery of a portfolio of clinical outcome assessment products. Responsibilities include preparing COA assets, defining deliverables and ROI, developing go-to-market and thought-leadership materials, supporting business cases and due diligence, coordinating with cross-functional teams, and maintaining delivery communications. The role requires life sciences or technical education, product or program management experience, strong communication skills, and at least four years of professional experience.

Analyzes healthcare, pharmacy, medical, payer, reimbursement, and claims adjudication data to identify trends, denials, access barriers, and actionable business insights. Produces validated datasets, reports, dashboards, and ad hoc analyses using IQVIA platforms. Ensures data accuracy and quality, audits analytical work, supports internal and client-facing projects, collaborates cross-functionally, and presents findings and recommendations to stakeholders.

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.