Clinical Research Associate Jobs in Connecticut, United States

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.

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.

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.

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.

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.

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.

In House Clinical Research Associate

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.

Clinical Research team at CTTX Health focuses on advancing innovative neuroscience therapies through rigorous clinical trials. The Clinical Research Associate conducts site initiation, monitoring, and close-out visits, verifies study data, and collaborates with site staff to resolve challenges and ensure protocol compliance.

Clinical Research Associate/Coordinator I at Mass General Brigham works with the oncology research team to enroll patients, manage data collection, and coordinate regulatory reporting. The role involves screening patients, scheduling tests, entering data, and liaising with sponsors and the IRB to ensure protocol compliance.

Clinical Research Associate at Mass General Brigham. Responsible for ensuring regulatory compliance of clinical trials, managing IRB submissions, maintaining study binders, handling adverse events, and supporting monitoring visits.

Clinical Research Associate/Clinical Research Coordinator I works independently under general supervision to consent and enroll eligible patients to translational research protocols, coordinate specimen collection, maintain patient databases, submit regulatory documents to IRB and sponsor, and monitor/report adverse events.

Mass General Brigham seeks a Clinical Research Associate/Clinical Research Coordinator I to enroll patients, manage data collection, coordinate specimen processing, and maintain regulatory compliance for translational cancer studies. The role involves patient consent, scheduling, data entry, and collaboration with clinical teams and sponsors.