Jobs at IQVIA

The Site Activation Specialist manages site documentation, coordinates regulatory activities, and serves as the primary contact for investigative sites, ensuring compliance with safety and effectiveness standards for clinical trials.

Provide Tier 2 technical support for Veeva applications, resolve escalated issues, perform root cause analysis, manage customer expectations, and document solutions. Collaborate with teams, monitor system performance, and stay updated on Veeva releases.

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.

As a Senior Data Engineer, you will design scalable data pipelines and mentor junior engineers, ensuring high-quality code and collaborating across teams to optimize analytics solutions.

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

The Quality Manager implements the global Quality Plan, ensures compliance with standards, manages quality improvement initiatives, and supports stakeholders in adherence to clinical practices and regulations.

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

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.

Oversee a clinical team supporting clinical studies, managing resources, personnel training, performance evaluation, quality assurance, and project allocations to ensure successful project execution.

The Senior Clinical Research Associate is responsible for monitoring site activities, managing clinical trials, ensuring compliance with regulations, and mentoring clinical staff.

The Senior Site Activation Coordinator manages site activation tasks, ensures compliance with regulations, reviews documentation, and updates internal systems to support clinical trials.

The Clinical Research Associate II monitors oncology clinical trials, conducts site visits, ensures compliance with regulations, and manages data integrity.

The Bilingual Customer Support Representative provides patient support in a call center environment, managing communications, offering clinical advice, and ensuring program compliance for Patient Support Solutions programs.

Responsible for managing multiple accounts in designated geographic areas or industries, meeting financial goals through client relationships and business development efforts.

Oversee and manage the QA program, ensuring compliance with regulations, providing support and training to development groups, and addressing audit findings while improving processes.

The Principal Biostatistician provides statistical support for early-phase drug development programs, focusing on healthy subjects with PK and PD endpoints. Responsibilities include collaborating with project teams, conducting analyses using SAS and/or R, and contributing to various clinical documents and reports.

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 Associate Consultant will provide high-quality analytical input for client projects in life sciences, assisting with problem analysis, developing solutions, and managing data. Responsibilities include analysis, presentation preparation, and managing multiple priorities in a collaborative environment.

The Staff Architect will lead technical vision and architectural strategy for MediaOS, ensuring scalable systems that align with business goals while mentoring teams and managing cross-product dependencies.

The Clinical Trial Educator will provide training and information about clinical trial criteria to coordinators and healthcare professionals, work with referral networks, and develop recruitment strategies, requiring frequent travel.