Clinical Research Associate Jobs in District of Columbia, United States

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 Associate - Medical Center

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.

Premier Research’s Global Clinical Monitoring and Site Management team builds the bridge between biotech, medtech, and specialty pharma companies and the patients who need new medicines. As a Clinical Research Associate I, you deliver quality monitoring reports, conduct site visits—remote or on‑site—ensuring data integrity and patient safety, and collaborate with the Clinical Lead to proactively resolve trial issues.

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.

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.

Clinical Research Associate at Georgetown University Medical Center provides clinical and research services to subjects in Infectious Diseases studies, manages complex COVID-19 trials, monitors and screens patients, administers investigational therapies, completes documentation, ensures protocol compliance, collaborates with clinical and research teams, and maintains high standards of patient care.

Clinical Research Associate at IQVIA Biotech partners with biotech companies to accelerate clinical development. Responsible for onsite monitoring of clinical trial sites, ensuring compliance with GCP, ICH, and sponsor protocols.

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 Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

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.

Clinical Operations team at AstraZeneca conducts global clinical studies. The Clinical Research Associate monitors site activities, ensures compliance with ICH‑GCP, conducts remote and onsite visits, and drives enrollment and data quality.

Clinical Research team at AstraZeneca conducts global clinical studies to develop innovative medicines. As a Field Based Clinical Research Associate you will manage study sites, ensure compliance with ICH/GCP guidelines, and collaborate with local study delivery teams to meet quality and timeline goals.

Clinical Research Team at AstraZeneca conducts global clinical studies to develop innovative medicines. The Field Based Clinical Research Associate manages site delivery, prepares, initiates, monitors, and closes study centers while collaborating with local teams to meet quality and timeline commitments.

Clinical Research team at AstraZeneca drives the development of innovative medicines by overseeing study execution across therapeutic areas. As a Field Based Clinical Research Associate you will manage the preparation, initiation, monitoring and closure of study sites, collaborating with monitors and local delivery teams to meet quality and timeline commitments.

Clinical Research team at AstraZeneca drives global clinical studies to bring innovative medicines to patients. The Field Based Clinical Research Associate manages study delivery at assigned sites, overseeing initiation, monitoring, and closure while ensuring compliance with ICH/GCP and local regulations.

Cell Therapy Site Management & Monitoring Organization at AstraZeneca builds and oversees cell therapy clinical studies. The CRA prepares, initiates, monitors, and closes study sites, conducts onsite and remote monitoring visits, manages study supplies, and ensures compliance with ICH‑GCP and local regulations.

IQVIA Biotech is hiring a Clinical Research Associate (CRA) to monitor and manage clinical sites, ensuring compliance with GCP, ICH guidelines, and regulatory requirements. The role requires a minimum of 1 year of on‑site monitoring experience (CRA 2) or 6 months (CRA 1) with oncology solid tumor focus.

Clinical Operations at Worldwide Clinical Trials drives innovative cardiovascular research across the East Coast. The Senior CRA manages site activities from start‑up to close‑out, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations while training sites on data collection and safety reporting.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior CRA will manage site activities for CNS/Neurology studies, conduct initiation visits, ensure regulatory compliance, and support contract and budget negotiations while collaborating remotely with West Coast sites.