Clinical Research Associate Jobs in Massachusetts, United States

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 role at Integrated Resources, Inc. supports clinical study operations, ensuring adherence to protocols and timelines. The CRA works closely with Clinical Project Managers, assisting in document preparation, vendor coordination, and monitoring report review.

The Senior Clinical Research Associate at Paragonix Technologies, Inc. reports to the VP Scientific and Medical Affairs and oversees prospective randomized clinical studies across solid organ platforms. Day-to-day responsibilities include providing data coordination and management, managing investigative site activity for multiple protocols, coordinating budgets and invoicing, creating and implementing subject enrollment strategies, designing CRFs and eCRFs, and supporting reporting to clinicalt

Clinical Research Associate role at Integrated Resources, Inc. supports day‑to‑day clinical study operations under the Clinical Project Manager. The CRA assists in authoring study documents, oversees CRO investigator background checks, manages vendor shipments, and ensures essential documents for investigational medicine release.

AstraZeneca seeks a Clinical Research & Development Associate Director in Gaithersburg, Maryland, to drive the development of novel therapies for inflammatory myopathies and related diseases. The role integrates clinical, scientific, and commercial expertise to oversee study design, execution, and lifecycle management while mentoring 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.

AstraZeneca seeks a Clinical Research & Development Associate Director for Myositis/Immunology in Gaithersburg, Maryland. This role drives the development of novel therapeutics for inflammatory myopathies and autoimmune diseases by integrating scientific, commercial, and operational strategies.

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.

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.

The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies. The CRA/CRC I will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting.

The Multicenter Program within the MGB Cancer Institute Clinical Trials Office is seeking candidates experienced in clinical trial coordination and implementation to support multicenter coordination and monitoring of investigator-initiated oncology clinical trials. The Multicenter Program is an internal clinical trial operations team, specializing in the central coordination, monitoring and regulatory oversight of MGBCI investigator-initiated clinical trials that are expanded to participating si

The Clinical Research Associate (CRA) supports clinical trial quality, compliance, and execution through site monitoring, study startup, data oversight, and regulatory documentation. The CRA will also serve as an in-house sponsor representative overseeing CROs and third-party monitoring vendors, ensuring delegated activities meet protocol, GCP, quality, and timeline requirements.

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Moderna is seeking an experienced and highly motivated Senior Research Associate to join the Clinical Biomarker Laboratory (CBL) Immunoassay and Cell Based Assay group. This laboratory-based role will support the development, qualification, validation, transfer, and clinical implementation of cell-based assays, virus neutralization/functional antibody assays, and ligand-binding assays (LBAs) used to characterize vaccine-induced immune responses and support clinical vaccine development programs,

Moderna is seeking an experienced and highly motivated Principal Research Associate to join the Clinical Biomarker Laboratory (CBL) Immunoassay and Cell Based Assay group. This laboratory-based role will primarily support the development, qualification, validation, and clinical implementation of ligand-binding assays (LBAs) and cell-based assay for biomarker and immunogenicity testing across Moderna's infectious disease, oncology, and autoimmune disease clinical programs.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Are you a visionary expert in clinical drug development, possessing the capabilities to drive a successful strategy in accelerating the development of cellular therapies for patients with immune-mediated diseases? Are you dedicated to revolutionizing the treatment of immune-mediated diseases and creating a significant impact on patients' lives?

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.

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US.