Jobs at IQVIA

Analyzes project requirements, develops and maintains SAS and SQL programs, documents code, performs quality assurance, formats results to client specifications, and supports monthly deliverables. The role requires working with large and longitudinal databases, producing ad hoc reports, managing multiple projects, and collaborating effectively with clients and team members.

Performs country- or region-level feasibility, site activation, and site maintenance activities for clinical studies. Prepares, reviews, distributes, and tracks regulatory, contractual, ethics, informed consent, and investigator documentation. Maintains project databases, tracking tools, timelines, and plans while coordinating with Site Activation Managers, project management, investigative sites, and internal teams to ensure document completeness, accuracy, approvals, and execution.

Leads complex consulting and analytics projects for pharmaceutical, biotechnology, life sciences, healthcare, and government clients. Responsibilities include managing multidisciplinary teams, conducting qualitative and quantitative analyses, developing strategic recommendations, presenting client deliverables, mentoring junior staff, managing senior client relationships, and identifying follow-on business opportunities. The role requires expertise in life sciences consulting, large datasets, project management, business analytics, and pharmaceutical market trends.

Directs strategic, operational, and financial site activation for clinical studies across multiple regions. Oversees site identification and selection, regulatory and ethics processes, contracting, study start-up, lifecycle maintenance, project plans, timelines, and stakeholder communications. Develops regulatory strategies, manages documentation and reporting, supports bids, ensures compliance with ICH-GCP and company standards, and mentors colleagues. Requires international experience and leadership in a scientific or clinical environment.

Conduct statistical programming for oncology clinical studies using SAS; create CDISC-compliant ADaM datasets, tables, listings, graphs, and ad hoc analyses. Validate programs and results, review CDISC validation outputs, support TLF shell and SAP preparation, and ensure compliance with ICH guidelines, company SOPs, and regulatory submission standards. Work independently across studies while coordinating with statisticians and programming colleagues.

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 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.

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