Clinical Research Associate Jobs in Massachusetts, 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.

In House Clinical Research Associate

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 Merck conducts oncology trials across the US. The Clinical Research Associate manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and collaborates with cross‑functional groups to drive study performance. Remote work, candidates must reside in listed states, travel 65‑75% of time, 2‑3 days/week on site.

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.

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.

Alliance for Clinical Trials in Oncology Foundation's Operations team drives large-scale cancer clinical research. The Clinical Research Associate supports site management, feasibility assessments, eTMF and CTMS oversight, and regulatory compliance across studies.

Clinical Research team at Mass General Brigham ensures regulatory compliance for clinical trials. The associate maintains study binders, prepares IRB submissions, manages adverse event documentation, and supports monitoring visits.

Clinical Research Associate at Mass General Brigham works within the clinical research team to manage regulatory submissions and data collection for multiple cancer studies. The role organizes study binders, prepares IRB documents, enrolls patients, abstracts data, and ensures compliance with federal and institutional regulations.

Clinical Research Associate/Coordinator I at Mass General Brigham enrolls patients for cancer studies, manages data collection, regulatory compliance, and communication with clinical teams, sponsors, and IRB. Works independently under general supervision, coordinates appointments, specimen collection, data entry, adverse event reporting, and audit preparation. Requires attention to detail, organizational skills, and knowledge of clinical research protocols.

Clinical Research Associate supports cancer studies by enrolling patients, managing data entry, and ensuring regulatory compliance. The role involves verifying consent, monitoring protocol adherence, reporting adverse events, maintaining study binders, coordinating sponsor visits, and resolving data queries.

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.

Mass General Brigham seeks a Clinical Research Associate Manager to oversee daily operations of clinical trials in anterior and posterior segment research. The role supervises 4‑8 staff members, manages project priorities, ensures protocol compliance, and collaborates with sponsors and investigators.

Clinical Research Associate/Coordinator I at Mass General Brigham supports translational research protocols by consenting and enrolling patients, coordinating specimen collection, and managing data entry and regulatory documentation. The role involves direct patient interaction, coordinating tissue and blood sample processing, scheduling tests, and maintaining an organized database of patient information.

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.

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.

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.