Clinical Research Associate Jobs in New York, United States

Clinical Research Associate on the Clinical Research team at New York Medical College, supporting pre‑clinical trial setup, regulatory submissions, IRB activities, patient screening, specimen handling, and data management. Role involves coordinating with PI, clinical staff, and research nurses to ensure protocol compliance and adverse event reporting.

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

VahatiCor is an early-stage cardiovascular medical device company developing breakthrough catheter-based Class III systems to improve outcomes for patients with coronary microvascular dysfunction. The Senior Clinical Research Associate owns site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor’s cardiovascular medical device trials, serving as the primary operational partner to clinical sites.

Preclinical Vector Design team at MeiraGTx develops and tests therapeutic vectors in mouse models and iPSCs. The Research Associate performs molecular characterization, cell culture assays, in‑vivo tissue processing, NGS library preparation, and data analysis to support a machine‑learning driven design pipeline.

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 Senior Clinical Research Associate I is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards. The Senior Clinical Research Associate I r ole is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. en

The Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards. The Clinical Research Associate r ole is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

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.

The Clinical Research Associate, In-House (IH) will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, support for process improvement, collection of essential documents and overall clinical trial support.

The Senior Clinical Research Associate II is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards. The Senior Clinical Research Associate II r ole is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.

Fortrea is seeking Experienced CRA 2s to lead and support its Full Service Outsourcing team across major US hub locations. In this role, you will apply clinical judgement to monitor clinical trial sites, ensure participant safety and data integrity, and respond to emergencies per clinical research standards.

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US.

IQVIA Biotech is expanding its Clinical Monitoring team and seeks CRA 2 professionals to ensure the successful execution of clinical trials for biotech sponsors. In this role, you will monitor and manage clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations, directly contributing to the integrity and quality of clinical research data.

The Sr. CRA II - General Medicine - East Coast or Mid-West role supports the Full Service Outsourcing team at Covance, reporting within the Fortrea Inc. organization. You will lead and support clinical trial operations by performing all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.

Adams Clinical is a clinical trial site network dedicated to accelerating life-changing medicines through uncompromising data quality, safety, and diverse enrollment. As a Clinical Research Nurse, you will work under physician principal investigators and a clinical nurse manager to conduct pharmaceutical-sponsored trials in compliance with FDA regulations and GCP guidelines.

Clinical Research team at The Dermatology Specialists drives patient enrollment for dermatology trials, blending rigorous clinical coordination with proactive recruitment. The Coordinator sources candidates across 60+ locations, conducts prescreening calls, obtains consent, manages IRB documentation, and performs phlebotomy while meeting enrollment targets in a hybrid schedule.