Clinical Research Associate Jobs in New York, United States

Clinical Monitoring team at Rho drives successful clinical trials by overseeing site management and data integrity. The Clinical Research Associate performs both onsite and remote monitoring, conducts 8-10 site visits per month, and ensures compliance with ICH GCP and FDA regulations.

Clinical Research Associate on Merck's Oncology team, responsible for ensuring compliance and performance of clinical trial protocols across assigned sites. The role conducts site monitoring, manages regulatory documentation, and collaborates with cross‑functional teams to support study start‑up, execution, and close‑out.

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

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.

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.

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.

Clinical Research team at Merck conducts oncology trials across the United States. The Clinical Research Associate ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional partners.

The Clinical Research Associate at AstraZeneca's Study Delivery team is based in New York City, New York, and holds local responsibility for delivering clinical studies at allocated sites. Day-to-day work includes preparing, initiating, monitoring, and closing sites in compliance with ICH-GCP and AZ Procedural Documents, performing monitoring visits and source data verification, managing study and drug supplies, updating CTMS and eTMF, and collaborating with the Local Study Team.

IQVIA Biotech is hiring a Clinical Research Associate (CRA) to monitor and manage clinical sites, ensuring compliance with GCP, ICH guidelines, and regulatory requirements. The role requires a minimum of 1 year of on‑site monitoring experience (CRA 2) or 6 months (CRA 1) with oncology solid tumor focus.

Clinical Research Team at NAMSA advances medical device safety by supporting clients throughout product development. The Senior Clinical Research Associate oversees study monitoring, site qualification, and regulatory submissions, ensuring GCP compliance and high-quality data.

Merck seeks a Clinical Research Associate to manage assigned protocols and sites within Immunology, ensuring compliance with ICH/GCP and country regulations. The role involves acting as the primary site contact, performing remote and on-site monitoring, and developing new clinical research territories across designated US locations.

Clinical Research Associate on the Cardiovascular/Vaccine/Infectious Disease team at Merck, responsible for ensuring protocol compliance and site performance across multiple US locations. The role monitors clinical sites, manages relationships, conducts site visits, and oversees data quality and patient safety while collaborating with cross‑functional teams.

Clinical Research team at Merck drives cardiovascular, vaccine, and infectious disease studies. The Clinical Research Associate monitors site compliance, manages study documentation, and builds strong site relationships across the United States.

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.

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.

Join a global clinical research organization that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

Endocrinology Diabetes and Metabolism team at Weill Cornell Medicine supports clinical research studies focused on metabolic disorders. The Clinical Research Assistant coordinates trial data management, assists with subject enrollment, maintains research charts, prepares lab kits, and reports adverse events, ensuring compliance with GCP and regulatory guidelines.

Division of Nutritional Sciences at Cornell Human Ecology conducts interdisciplinary research on women's health and nutrition. The Clinical Research Coordinator manages multi-site human studies, leading participant recruitment, biospecimen handling, data management, and compliance with IRB and funding agencies.