Clinical Research Associate Jobs in Virginia, 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.

Fortrea's FSP team is seeking a Clinical Research Associate 2 to deliver high-standard clinical trial monitoring across Ohio, Pennsylvania, or Virginia. Day-to-day, you will manage all aspects of site monitoring (routine and close-out), conduct pre-study and initiation visits, verify informed consent and protocol adherence, review CRFs and resolve queries, handle SAE reporting, and support registry management and feasibility work.

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.

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health.

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.

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

The Clinical Research Coordinator supports clinical research studies within the Department of Obstetrics and Gynecology in Norfolk, VA. Day-to-day work includes participant recruitment and enrollment, obtaining informed consent, collecting and managing research data, coordinating study visits, maintaining regulatory files, and serving as a liaison between investigators, participants, and clinical staff. This full-time position is coterminous with research funding.

The Clinical Research Coordinator I supports high-quality clinical research at the Newport News, VA location. This part-time role manages study protocols, patient enrollment, and regulatory compliance while coordinating with medical teams and sponsors.

Operations team at Alcanza Clinical Research coordinates multi-site clinical studies across therapeutic areas. The Clinical Research Coordinator II manages patient screening, consent, visits, data entry in EDC, specimen handling, and regulatory documentation while ensuring compliance with FDA, GCP, and HIPAA.

Riverside Health System Clinical Research team conducts clinical trials to advance medical knowledge and patient care. The Registered Nurse Clinical Research Coordinator manages trial logistics, ensures regulatory compliance, maintains accurate data in the CTMS, and supports patient enrollment and safety monitoring.

Nursing Solutions Group at Science 37 builds mobile clinical nurse services for decentralized trials. The Per Diem Mobile Research Nurse delivers patient care at participants’ homes, collaborates with brick‑and‑mortar sites, and supports trial implementation across therapeutic areas.

Per Diem Clinical Research Nurse – Home Visits at Science 37’s Nursing Solutions Group. The team delivers mobile clinical nurse services to participants in decentralized clinical trials, collaborating with clinicians, researchers, and tech developers to ensure compliant, high‑quality care.

Science 37’s Nursing Solutions Group builds mobile clinical nurse services for decentralized clinical trials. The Mobile Research Nurse delivers patient care at participants’ homes, collaborates with brick‑and‑mortar sites, and ensures compliance with GCP and SOPs.

The Clinical Site Manager is responsible for overseeing performance of the research site activities. Provides on-site oversight to help ensure execution and coordination of clinical research activities visits, documentation and follow up actions according to ICH/FDA guidelines, GCP, and company SOPs, policies and procedures.

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Clinical Research Coordinator I conduct high quality clinical research following the highest ethical and regulatory standards of care. This is a part-time position with a typical schedule of Monday through Thursday , either 7:00 AM–1:00 PM or 8:00 AM–2:00 PM .

Sentara Heart Hospital located on the campus of Sentara Norfolk General Hospital is seeking a Clinical Research Assistant. The Clinical Research Assistant will be responsible for assisting the Clinical Research Coordinators with the clinical trials; including the following activities: screening, enrolling, patient follow-up and study-related data entry.

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine.

Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator III (RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work.