Clinical Research Associate Jobs in New York, United States

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.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

Premier Research seeks a Clinical Research Associate II for the NorthEast Dermatology region to join its Global Clinical Monitoring and Site Management team. The role involves monitoring Phase I‑IV clinical trials, ensuring data integrity and patient safety per ICH‑GCP/ISO 141155, serving as primary site contact, managing queries, supporting Trial Master File activities, and attending investigator meetings.

Premier Research seeks a Clinical Research Associate II to join its Global Clinical Monitoring and Site Management team. The role involves monitoring Phase I‑IV trials across neuroscience, oncology, rare, and cardiovascular studies, ensuring data integrity per ICH‑GCP/ISO 141155, and serving as the primary contact for investigative 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.

Clinical Research team at Merck conducts immunology trials, ensuring protocol compliance and patient safety. The CRA manages site relationships, performs remote and onsite monitoring, and oversees regulatory documentation across multiple US locations.

Clinical Research Operations at Merck conducts cardiovascular, vaccine, and infectious disease trials. The Clinical Research Associate monitors site performance, ensures compliance with ICH/GCP, manages documentation, and supports site selection and expansion.

FSP Clinical Research Team conducts oncology trials to advance cancer therapies. The CRA monitors study sites, conducts pre‑study and initiation visits, ensures protocol compliance, reviews CRFs, reports serious adverse events, and supports site staff.

Clinical Research team at AstraZeneca ensures the delivery of clinical studies at allocated sites, overseeing study initiation, monitoring, and closure in compliance with AZ SOPs and ICH‑GCP. The Clinical Research Associate monitors sites, updates CTMS, manages study drug supplies, conducts source data verification, and trains investigators while collaborating with local study managers.

Clinical Research Associate II - Neuro & Immunology role at AbbVie focuses on advancing the company's pipeline by ensuring high‑quality clinical trial execution and site engagement. The CRA II partners with investigators and site staff to monitor trials, train sites, and drive data integrity and compliance across neuro and immunology studies.

Clinical Research Associate II on AbbVie’s Neuro & Immunology team, advancing the pipeline by ensuring rigorous site clinical research and data integrity. The role serves as the primary site contact, training and motivating investigators, conducting monitoring and risk assessments, and leveraging CRM tools for engagement.

Clinical Research Associate at IQVIA Biotech partners with biotech companies to accelerate clinical development. Responsible for onsite monitoring of clinical trial sites, ensuring compliance with GCP, ICH, and sponsor protocols.

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.

Cell Therapy Site Management & Monitoring team ensures clinical study sites deliver high-quality data and compliance across New York and New Jersey. The Clinical Research Associate monitors site initiation, conduct and closure, performs source data verification, manages study supplies and updates CTMS, while training investigators and ensuring regulatory adherence.

Clinical Research team at Merck conducts oncology trials to advance new therapies. The CRA manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and documents study activities across the United States.

Clinical Research team at Merck conducts cardiovascular studies, ensuring protocol compliance and patient safety across multiple sites. The Clinical Research Associate manages site relationships, performs remote and onsite monitoring, and collaborates with cross‑functional groups to drive study execution.

IQVIA’s Clinical Research Associate team drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts site visits, manages recruitment plans, administers protocol training, and maintains Trial Master File documentation across multiple U.S. locations.

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’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.

IQVIA Biotech team in the Clinical Research Associate I role drives site monitoring and data integrity for oncology, cardiovascular, metabolic, and renal studies. The role conducts site selection, initiation, monitoring, and close‑out visits, collaborates with study teams, and manages regulatory submissions and enrollment tracking.