Clinical Research Associate Jobs in New Jersey, United States

Clinical Monitoring team at Rho drives successful clinical trials by overseeing site management and data integrity. The Clinical Research Associate performs both onsite and remote monitoring, conducts 8-10 site visits per month, and ensures compliance with ICH GCP and FDA regulations.

Clinical Research Associate on Merck's Oncology team, responsible for ensuring compliance and performance of clinical trial protocols across assigned sites. The role conducts site monitoring, manages regulatory documentation, and collaborates with cross‑functional teams to support study start‑up, execution, and close‑out.

Lead Clinical Research Associate role at Integrated Resources, Inc. The position oversees field monitor performance, ensuring adherence to protocols, GCP, ICH, and federal regulations. Responsibilities include developing enrollment strategies, vendor selection, monitoring plan execution, trip report review, scheduling, metrics tracking, issue escalation, training material creation, and adjudication committee support.

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 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 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’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 Research team at Merck conducts oncology trials across the United States. The Clinical Research Associate ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional partners.

Clinical Research team at Merck conducts cardiovascular trials to advance therapeutic innovation. The CRA ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional groups.

Merck seeks a Clinical Research Associate to manage assigned protocols and sites within Immunology, ensuring compliance with ICH/GCP and country regulations. The role involves acting as the primary site contact, performing remote and on-site monitoring, and developing new clinical research territories across designated US locations.

<p style="text-align:left"><b>Job Description</b></p><p style="text-align:inherit"></p><p><b><u>CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS</u>: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA</b></p><p></p><p>The role is accountable for performance and compliance for assigned protocols and sites in a country.</p><p></p><p>Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company

Merck seeks a Clinical Research Associate specializing in Oncology to manage assigned clinical trial sites and ensure regulatory compliance. The role involves conducting remote and on-site monitoring, developing site relationships, and acting as a subject matter expert for monitoring processes.

Translational Medicine (TMed) drives early clinical development of novel therapeutics by translating scientific discoveries into human proof-of-concept and advancing candidates through the pipeline. The Associate Principal Scientist, Clinical Research (Early Clinical Scientist) provides operational and scientific leadership for the design, planning, and execution of early-phase clinical trials and vaccine programs, overseeing cross-functional teams, ensuring GCP/ICH compliance, and authoring cli

The Associate Clinical Research Manager (aCRM) - Lung at Merck & Co., Inc. (Rahway, NJ) is accountable for end-to-end project management and performance of assigned clinical trial protocols within a country, ensuring compliance with ICH/GCP and local regulations. Day-to-day, the role serves as the main point of contact between Country Operations and the clinical trial team, drives feasibility, site selection, recruitment, execution, and close-out, reviews monitoring visit reports, leads local st

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.

Clinical Research team at Merck conducts cardiovascular studies, ensuring protocol compliance and patient safety across multiple sites. The Clinical Research Associate manages site relationships, performs remote and onsite monitoring, and collaborates with cross‑functional groups to drive study execution.