Clinical Research Associate Jobs in Massachusetts, 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.

Alliance for Clinical Trials in Oncology Foundation (Alliance) conducts large-scale cancer clinical trials to advance treatment and prevention. The Clinical Research Associate supports study start‑up and site management, handling feasibility assessments, eTMF filing, CTMS data entry, and coordination with CROs and investigators.

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 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.

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

Translational Medicine (TMed) drives early clinical development of novel therapeutics by translating scientific discoveries into human proof-of-concept and advancing candidates through the pipeline. The Associate Principal Scientist, Clinical Research (Early Clinical Scientist) provides operational and scientific leadership for the design, planning, and execution of early-phase clinical trials and vaccine programs, overseeing cross-functional teams, ensuring GCP/ICH compliance, and authoring cli

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.

Paragonix Technologies, part of Getinge, develops organ transportation and preservation devices. The Senior Clinical Research Associate oversees prospective randomized clinical studies, managing data coordination, site activity, and budget invoicing across solid organ platforms.

<p style="text-align:left"><b>Job Description</b></p><p style="text-align:inherit"></p><p><b><u>CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS</u>: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA</b></p><p></p><p>The role is accountable for performance and compliance for assigned protocols and sites in a country.</p><p></p><p>Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company

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.

Moderna's Clinical Flow Cytometry group seeks a Senior Research Associate to serve as a technical expert generating high-parameter flow cytometry data under GCLP guidelines to support clinical programs across multiple therapeutic areas. Day-to-day work includes developing and validating cell-based flow cytometry assays, executing clinical sample testing, performing ex vivo stimulation and intracellular cytokine staining on PBMCs, and analyzing data with FCSExpress.

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.

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.

Clinical Research Coordinator supports multiple trials at BIDMC, overseeing recruitment, screening, enrollment, consent, data entry, protocol compliance, and regulatory documentation. Requires 1‑2 years experience, medical terminology, computer skills, and fluency in Spanish/Portuguese.

The Cancer and Hematology Clinical Research Program at Boston Medical Center seeks a Clinical Research Coordinator II to support biomedical research in Boston. This on-site role involves managing patient recruitment, obtaining informed consent, abstracting medical records, and maintaining regulatory files for clinical studies.

Oncology Clinical Development – Hematology team drives the design and execution of clinical research for new and marketed oncology medicines. The Senior Clinical Director leads end‑to‑end clinical development, overseeing trial design, regulatory strategy, data analysis, and cross‑functional collaboration.

Clinical Research Assistant II on CARE at Beth Israel Deaconess Medical Center, the team that drives anesthesia research and clinical trials. The role screens, enrolls, and monitors patients, ensures protocol compliance, extracts data, and coordinates insurance and IRB activities.

The Clinical Director (Principal Scientist) in the Hematology Section of the Oncology therapeutic area leads clinical research activities for new and marketed medicines across all phases of clinical development. Day-to-day, the role plans and directs clinical trials, provides medical oversight, analyzes and summarizes clinical findings, collaborates with cross-functional teams, and supports business development assessments.