Clinical Research Associate Jobs in Virginia, 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 Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas, including Oncology. The Clinical Research Associate II manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting data collection and safety reporting.

Clinical Operations at Worldwide Clinical Trials drives scientific breakthroughs by managing multi‑therapeutic clinical studies. The Clinical Research Associate II, Psychiatry, oversees site activities, conducts initiation visits, ensures regulatory compliance, and trains sites on data collection, all while supporting psychiatric monitoring.

Worldwide Clinical Trials is a global CRO seeking a Clinical Research Associate (Bilingual) – Oncology to support non-interventional studies across Canada. The role involves managing site research activities, from site identification and start‑up to data collection, safety reporting, and study close‑out.

IQVIA’s Clinical Research Associate team drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts site visits, manages recruitment plans, administers protocol training, and maintains Trial Master File documentation across multiple U.S. locations.

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.

IQVIA’s Clinical Research team drives site monitoring to ensure compliance with GCP and ICH. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files. Based in Overland Park, KS with additional sites in Durham, NC; Parsippany, NJ; and Carlsbad, CA, the position is on-site with a hybrid travel component.

IQVIA’s Clinical Research team drives site monitoring and data integrity for clinical trials. The Associate conducts GCP‑compliant site visits, manages recruitment plans, and ensures accurate CRF submission.

IQVIA Biotech team in the Clinical Research Associate I role drives site monitoring and data integrity for oncology, cardiovascular, metabolic, and renal studies. The role conducts site selection, initiation, monitoring, and close‑out visits, collaborates with study teams, and manages regulatory submissions and enrollment tracking.

IQVIA seeks a Clinical Research Associate 2 with on‑site monitoring experience in CNS, GLP‑1/Obesity/Diabetes (Type II) and/or Cardiovascular trials. Responsibilities include site monitoring visits, recruitment planning, protocol training, quality assessment, regulatory submissions, TMF/ISF maintenance, documentation, and financial management.

IQVIA seeks a Clinical Research Associate 2 to conduct on‑site monitoring in IM/GI, MASH/NASH, dermatology and asthma/respiratory trials. Responsibilities include site visits, recruitment tracking, training, quality evaluation, regulatory submissions, documentation, liaison with study teams, and financial management.

Perform site monitoring visits, manage study progress, ensure compliance with GCP/ICH, maintain TMF/ISF, generate reports, support recruitment, handle financials, and collaborate with study teams.

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.

Perform site monitoring and management to ensure compliance with GCP/ICH and sponsor protocols. Drive recruitment, administer training, evaluate site quality, track regulatory submissions, CRF completion, data queries, and financial invoices.

Perform monitoring and site management to ensure study sites conduct protocols and report data per GCP, ICH, and sponsor requirements. Conduct site monitoring visits (selection, initiation, monitoring, close‑out), adapt recruitment plans, administer protocol training, evaluate site practices, manage regulatory submissions, recruitment, CRF completion, data queries, and TMF/ISF documentation.

IQVIA is hiring Clinical Research Associates (CRA) at the 1 and 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology.

Job Overview 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. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Clinical Research Associate, Sponsor Dedicated, Oncology or Immunology – Join IQVIA’s global clinical research team to manage site operations, ensuring compliance with GCP and ICH guidelines. In this role you will conduct site selection, initiation, monitoring, and close‑out visits, develop recruitment plans, provide protocol training, and maintain communication with study sites.

Clinical Research Associate, Sponsor Dedicated at IQVIA supports clinical trials by monitoring sites, ensuring compliance with GCP and ICH guidelines, and managing study documentation. The role involves conducting site initiation, monitoring, and close‑out visits, coordinating recruitment plans, and tracking regulatory submissions.

Clinical Research Associate, Sponsor Dedicated, Oncology – responsible for ensuring clinical trial sites operate smoothly, conducting site visits, monitoring compliance with GCP and ICH, managing recruitment, training, documentation, and financials. Works closely with study teams to support project execution and maintain high-quality standards across multiple locations.