Clinical Research Associate Jobs in New Jersey, United States

The Clinical Research Associate will oversee site monitoring and operational support across multiple domestic and international clinical trials. Reporting to the Associate Director of Clinical Operations, the role ensures adherence to SOPs, GCP, and regulatory requirements.

IQVIA’s Clinical Research team drives site monitoring and data integrity for clinical trials. The Associate conducts GCP‑compliant site visits, manages recruitment plans, and ensures accurate CRF submission.

Clinical Research Associate role at Integrated Resources, Inc. supports multiple domestic and international trials, overseeing site monitoring, budget tracking, and regulatory compliance. The position reports to the Associate Director of Clinical Operations and involves managing CRO activities, drafting protocols, and maintaining trial master files.

Terumo Medical Corporation (TMC), part of Tokyo-based Terumo Corporation, develops and markets medical devices across its Terumo Interventional Systems and Terumo Medical Products divisions. The Senior Clinical Research Associate supports day-to-day clinical trial execution by monitoring multiple sites and studies, ensuring data quality, site adherence to protocol/GCP/regulations, and serving as the primary liaison between clinical investigators and Terumo.

Lead Clinical Research Associate role at Integrated Resources, Inc. The position oversees field monitor performance, ensuring adherence to protocols, GCP, ICH, and federal regulations. Responsibilities include developing enrollment strategies, vendor selection, monitoring plan execution, trip report review, scheduling, metrics tracking, issue escalation, training material creation, and adjudication committee support.

IQVIA’s Clinical Research team drives site monitoring to ensure compliance with GCP and ICH. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files. Based in Overland Park, KS with additional sites in Durham, NC; Parsippany, NJ; and Carlsbad, CA, the position is on-site with a hybrid travel component.

IQVIA is seeking a Clinical Research Associate, Sponsor Dedicated, Oncology to ensure study sites operate smoothly and advance groundbreaking research. Day-to-day duties include conducting site visits, tracking recruitment and study progress, maintaining regulatory documentation, and mentoring clinical staff.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

FSP team seeks a Senior Clinical Research Associate II, Oncology to oversee clinical trial monitoring and site management. The role conducts site visits, ensures protocol compliance, reviews CRFs, and handles adverse event reporting while coordinating with vendors and training staff.

The Associate Clinical Research Director role within Sanofi's R&D organization supports the immunohematology Sickle Cell Disease development program by providing medical expertise and contributing to clinical development strategy. Day-to-day work includes supporting protocol and synopsis development, feasibility assessments, medical monitoring, clinical data review, risk assessment, and site engagement while collaborating with Clinical Leads, CRDs, investigators, and cross-functional teams.

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and externally.

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally.