Clinical Research Associate Jobs in North Carolina, United States

IQVIA Early Clinical Development team drives Phase 1 trials across diverse therapeutics. The Senior CRA monitors sites, ensures GCP compliance, tracks enrollment, manages TMF/ISF, and collaborates with cross‑functional teams in Durham, NC, onsite.

Clinical Research Associate I – Thermo Fisher Scientific, part of the global clinical operations team that supports pharmaceutical and biotech trials. The role conducts remote and on‑site monitoring visits, ensures protocol compliance, manages documentation, and collaborates with investigative sites to maintain data integrity.

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.

ProPharma Group, a consulting firm advancing biotech and pharmaceutical breakthroughs, seeks a Senior Clinical Research Associate to oversee monitoring and site management for clinical trials. The role conducts in‑person and remote monitoring visits, prepares reports, manages investigational supplies, and ensures regulatory compliance.

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.

PPD™ clinical research business of Thermo Fisher Scientific partners with pharma, biotech, and CROs to bring therapies to market. The Associate Contract Manager leads regional contract template preparation, negotiation and grant budget oversight, ensuring risk management and compliance.

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

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.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the Central Region to deliver high-standard clinical trial monitoring and participant care across a remote territory spanning multiple states. Day-to-day, the role covers full-cycle site monitoring, pre-study and initiation visits, CRF review and query resolution, SAE reporting, and registry management, with 8-10 on-site days per month.

The FSP team seeks a Clinical Research Associate 2 to ensure high standards of care and protocol adherence for participants in clinical trials. This role involves comprehensive site monitoring, data integrity verification via CRF review, and Serious Adverse Event reporting across California or Colorado.

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.

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 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 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.

IQVIA seeks a Clinical Research Associate to ensure sites conduct studies and report data per protocol, regulations, and sponsor requirements. The role involves performing site monitoring visits, managing recruitment plans, and maintaining regulatory documentation like the Trial Master File.

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.

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.

Duke Clinical Research Institute (DCRI) advances translational science by managing multi-site clinical trials. The Clinical Research Associate leads the site management and monitoring team, overseeing study setup, risk‑based monitoring, and regulatory compliance across assigned projects.

The Assistant Clinical Research Associate (ACRA) role supports FSP projects in liaison with the CRA and study Clinical Lead, contributing to site preparedness, logistical support for monitoring, and remote site management activities in accordance with SOPs and regulatory guidelines. Day-to-day duties include completing study and site management tasks per the task matrix, performing remote EMR/EHR checklist reviews, verifying document collection and RCR submission status, supporting site payments

Clinical Operations at Worldwide Clinical Trials drives innovative CRO solutions across therapeutic areas. The Senior Clinical Research Associate manages site activities for CNS and Oncology studies, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations, primarily remotely while residing in the Midwest.