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IQVIA is hiring a Clinical Research Associate, Sponsor Dedicated to monitor clinical trial sites and ensure study conduct and data reporting comply with protocols, regulations, guidelines, and sponsor requirements.

IQVIA’s Regulatory Science & Strategy team supports pharmaceutical, biotechnology, and medical device clients with regulatory challenges throughout the product lifecycle.

Responsibilities Enters data, extracts data via computer reports, analyzes reports, and shares analyses with management. Works closely with other departments in quality improvement activities.

IQVIA Laboratories is hiring a Sample Prep Scientist to prepare biological samples, solutions, and reagents for analytical testing in a regulated laboratory environment.

IQVIA is hiring an Associate Consultant to support regulatory science and strategy consulting engagements for pharmaceutical, biotechnology, and medical device clients.

MCRA, part of IQVIA MedTech, is hiring a Contract Virtual Clinical Coordinator to support the execution of clinical research studies through remote clinical activities.

ApTask Global Workforce (AGW) is recruiting for a global biotechnology company. The Quality Specialist supports the Corporate Quality Management System team by owning and approving deviation and CAPA records, supporting the deviation management system, and…

Green Key Resources is recruiting for a Long Island-based managed services provider. The Level 2 support role provides day-to-day client technical support, troubleshooting, and assistance with infrastructure and cloud technology projects.

Kashable is a FinTech company providing workplace financial wellness solutions. The IT Systems Administrator I provides first-line technical support to employees, manages accounts and equipment, and supports secure, compliant IT operations.

IQVIA is hiring a Site Activation Coordinator to perform country-level site activation activities for clinical studies in accordance with regulations, SOPs, and project requirements.

Responsibilities You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits Manage 2–6 trials of…

Responsibilities Apply standard modules/templates for ingestion and transformation, contributing consistent, reusable components Automate validations, quality checks, and repeatable runbook steps via scripting; support CI/CD workflows for routine deployments…

Responsibilities Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion Organizes research information for clinical trials Observes subjects and assists with data analysis…

Responsibilities Assists with coordinating all aspects of patient involvement from study initiation until study completion Organizes research information for clinical trials Observes subjects and assists with data analysis and reporting Schedules the…

Responsibilities Assists with coordinating all aspects of patient involvement from study initiation until study completion Organizes research information for clinical trials Observes subjects and assists with data analysis and reporting Schedules the…

Responsibilities Receive investigational product shipments for 300+ research protocols Document receipt of each shipment via sponsor acknowledgement of receipt form or email (as requested by sponsor) Upload temperature tracker data for each shipment (per…

UCSF Health is hiring a Clinical Research Coordinator for the POST SCD program. The role coordinates clinical research studies on sudden cardiac death, including participant and family engagement, data and specimen management, study reporting, staff training,…

Medix is seeking a Clinical Research Coordinator to manage ophthalmology and retina clinical trial operations in Denver.

VIA develops secure data exchange and trustworthy AI software for defense, public safety, and humanitarian organizations.

Parexel is seeking a Clinical Scientist to support the clinical and scientific conduct of oncology clinical studies.