Clinical Research Associate Jobs in Maryland, United States

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.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for rare CNS studies, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations.

The Contract Senior Clinical Research Associate (CRA) conducts site monitoring responsibilities for clinical trials, according to Standard Operating Procedures (SOPs), FDA regulations, ICH guidelines, and Good Clinical Practices (GCP).

The Contract Senior Clinical Research Associate (CRA) conducts site monitoring responsibilities for clinical trials, according to Standard Operating Procedures (SOPs), FDA regulations, ICH guidelines, and Good Clinical Practices (GCP).

We are seeking a Clinical Research Associate (CRA) with Ophthalmology monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.

We are seeking a Clinical Research Associate (CRA) with oncology monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.

We are seeking a Clinical Research Associate (CRA) with Metabolic/MASH or Obesity monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.

Professional Services team at Axle supports NIH research initiatives, focusing on clinical studies within the National Institute on Drug Abuse. The Clinical Research Coordinator manages participant recruitment, consent, data collection, and regulatory documentation, and assists with scheduling, travel arrangements, and sample handling.

CenExel CBH (CBH Health, LLC) in Gaithersburg, MD is a nationwide clinical research site and patient network specializing in CNS and early phase studies. The Clinical Research Coordinator I assists with coordinating clinical trials from study initiation to completion, organizing research information, observing subjects, scheduling data collection, documenting adverse events and protocol deviations, and performing safety and efficacy assessments per protocol.

National Institute of Neurological Disorders and Stroke (NINDS) team at NIH coordinates patient recruitment, scheduling, travel, and inpatient/outpatient admissions for clinical studies. The coordinator manages protocol documentation, regulatory binders, and data collection while acting as a liaison between patients, families, and research staff.

About the Position The Research Coordinator I oversees and administers research study and associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed.

National Cancer Institute Office of the Clinical Director team provides infrastructure for high‑quality intramural oncology research at NIH. The Clinical Research Coordinator manages study supplies, collects and validates data, and serves as the primary contact for participants while coordinating protocol‑required visits and regulatory documentation. Bethesda, MD, on‑site role supporting multiple cancer trials with occasional travel to study sites.

Arizona Arthritis & Rheumatology Associates, P.C. (AARA), the largest private rheumatology practice in the U.S., is hiring a Clinical Research Regional Manager to oversee clinical research staff and daily operations at assigned medical clinics. The role involves daily travel to research sites to manage, train, and mentor coordinators and assistants, monitor productivity and data metrics, ensure regulatory compliance, and serve as the escalation point for site staff.

Senior Clinical Research Coordinator oversees and administers clinical research studies, manages budgets, reviews protocols, and ensures compliance with GCP, CFR, and ICH guidelines. Coordinates study initiation, data collection, and analysis, recruits and manages research subjects, and serves as liaison with investigators, sponsors, and regulatory bodies.

Headlands Research Clinical Research team supports clinical trial delivery across community sites, leveraging technology and support services to expand patient participation. Clinical Research Assistants help execute trials by assisting with study visits, preparing materials, collecting and organizing data, and ensuring protocol compliance while interacting directly with patients and care teams.

Headlands Research Clinical Research team advances new therapies by managing patient-focused clinical trials across a growing network of sites. Coordinators support day-to-day trial execution, including patient interactions, study visit scheduling, data collection, and regulatory compliance while collaborating with investigators and cross‑functional teams.

The Research Coordinator in the Clinical Trials Unit collaborates with the Principal Investigator and research collaborators on studies of neurological, neurogenetic, neurodevelopmental, and psychiatric conditions in children, adolescents, and adults. Day-to-day duties include preparing IRB and regulatory documentation, supporting clinical trial activities such as participant recruitment and scheduling, managing research data, communicating with sponsors and vendors, and assisting with administr

The Research Coordinator position within the Clinical Trials Unit supports the Principal Investigator and research collaborators on studies of neurological, neurogenetic, neurodevelopmental, and psychiatric conditions across children, adolescents, and adults. Day-to-day work includes preparing IRB and regulatory documentation, coordinating clinical trial activities such as participant recruitment and scheduling, managing and analyzing research data, communicating with sponsors and vendors, and a

Under the direction of the Principal Investigator (PI), within the scope of nursing practice, and with minimal supervision, assesses, plans, and implements the safe and effective nursing care to Clinical Trials participants from pre-screening through study exit. Duties may include but are not limited to patient screening and enrollment, data collection forms, handling and supervision of specimens, data submission, and preparation of reports.

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