Jobs at IQVIA

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 Clinical Scientist will oversee and ensure data quality in clinical trials, conduct protocol reviews, develop training materials, and communicate with stakeholders.

Serve as a client-focused technology analyst for life sciences customers: gather and analyze requirements, design and deliver data-driven solutions, create documentation and client reports, recommend improvements, support client satisfaction and identify business opportunities while developing consulting and market expertise.

Client-focused Technology Analyst responsible for designing, developing and delivering data and technology solutions for life sciences clients. Reviews requirements, performs qualitative/quantitative analyses, crafts documentation and client presentations, supports solution implementation, and follows up to ensure client satisfaction. Develops consulting skills, market knowledge, and begins to build practice-specific subject matter expertise while identifying business opportunities.

Manage country-level site activation and global site feasibility studies (CRO- or sponsor-led) across Phase 1–3. Serve as SPOC for sites and project teams, prepare and QC regulatory/site documents, maintain tracking systems, monitor site performance, support project timelines and contingency plans, and improve feasibility processes. Work independently and may liaise directly with sponsors.

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 Product Strategist will lead digital engagement solutions, develop new capabilities, manage client relationships, and ensure high satisfaction while leveraging data and analytics for marketing strategies.

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

Provide advanced technical support for Veeva applications, resolving issues, managing environments, and ensuring optimal performance for Life Sciences clients. Collaborate with teams and document processes while staying updated on Veeva products.

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.