Clinical Research Associate Jobs in North Carolina, United States

Thermo Fisher Scientific’s Clinical Research team drives global oncology and ophthalmology trials. The Associate II monitors sites, ensures ICH‑GCP compliance, and manages risk‑based monitoring activities.

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.

This role oversees clinical trial site monitoring and management, ensuring compliance with GCP and ICH guidelines. Responsibilities include conducting site visits, evaluating site performance, maintaining trial documentation, and collaborating with study teams to support recruitment and data quality.

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 Research Associate (CRA) role at IQVIA, responsible for site selection, initiation, monitoring, close-out visits, documentation, recruitment plan support, communication, protocol training, quality evaluation, regulatory submission tracking, recruitment, CRF completion, data query resolution. Requires Bachelor's in health care or scientific discipline, 2 years of clinical research coordinator experience preferred, or CRA trainee program completion.

Clinical Research Associate - Sponsor Dedicated role at IQVIA involves monitoring and site management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site monitoring visits, managing recruitment plans, administering protocol training, evaluating site quality, tracking regulatory submissions, maintaining Trial Master File documentation, and collaborating with study teams.

Clinical Research Associate responsible for monitoring and site management to ensure compliance with protocols, regulations, and sponsor requirements. Conducts site visits, manages recruitment, training, documentation, and quality issues.

Clinical Research Associate role at IQVIA focuses on on‑site monitoring of GLP‑1/Obesity/Diabetes (Type II) trials. Responsibilities include performing site visits, managing recruitment, administering protocol training, ensuring compliance with GCP and ICH guidelines, tracking regulatory submissions, maintaining Trial Master File documents, and collaborating with study teams.

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.

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’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.