Clinical Research Associate Jobs in Pennsylvania, 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.

Krystal Biotech’s Clinical Operations team in Pittsburgh builds and manages gene‑therapy trials. The Clinical Trial Associate coordinates supply logistics, monitors GCP compliance, and trains site staff while traveling up to 50% of the time.

Olympus seeks a Senior Clinical Research Associate to manage clinical trials for medical devices and pharmaceuticals, ensuring compliance with GCP and FDA regulations. The role involves site monitoring, protocol development, and mentoring junior staff within a remote-first environment.

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 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.

<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

Fortrea's FSP team is seeking a Clinical Research Associate 2 to deliver high-standard clinical trial monitoring across Ohio, Pennsylvania, or Virginia. Day-to-day, you will manage all aspects of site monitoring (routine and close-out), conduct pre-study and initiation visits, verify informed consent and protocol adherence, review CRFs and resolve queries, handle SAE reporting, and support registry management and feasibility work.

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

FSP team seeks a Senior Clinical Research Associate II, Oncology to oversee clinical trial monitoring and site management. The role conducts site visits, ensures protocol compliance, reviews CRFs, and handles adverse event reporting while coordinating with vendors and training staff.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, Psychiatry, 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 multi‑therapeutic clinical studies, including oncology, by managing site activities and ensuring regulatory compliance. The Senior Clinical Research Associate oversees site start‑up, monitoring, data collection, safety reporting, and study close‑out, primarily remotely while coordinating with sites across the Northeast and Midwest.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

Responsible for the overall clinical research financial management and other financial matters of the School/Center. Will manage proposal development, budget development and related pre-award activities for diverse clinical research sponsor portfolio.

Office of Research and Innovation at Lehigh Valley Health Network coordinates advanced clinical trials, ensuring high‑quality patient care across multiple disease processes. The Clinical Research Coordinator II plans, implements, and monitors trial activities, manages patient assessments, phlebotomy, drug administration, and regulatory documentation.

Clinical Safety Team at Castle Biosciences ensures participant protection and regulatory compliance for FDA‑regulated LDT, IVD, and medical device studies. The Clinical Research, Clinical Safety Manager establishes and continuously improves safety processes, oversees adverse event management, risk assessments, safety reporting, and regulatory documentation, while partnering with cross‑functional teams to maintain inspection readiness.

The Clinical Research Nurse Sr. - Oncology Research at Thomas Jefferson University serves as a departmental and disease team resource for research protocol initiation and implementation within the oncology research area. Day-to-day, the role performs basic nursing skills, study coordination, and data management with a central focus on managing subject recruitment and enrollment, ensuring consistency of study implementation, data integrity, and compliance with regulatory requirements.

The Clinical Director (Principal Scientist) in the Hematology Section of the Oncology therapeutic area leads clinical research activities for new and marketed medicines across all phases of clinical development. Day-to-day, the role plans and directs clinical trials, provides medical oversight, analyzes and summarizes clinical findings, collaborates with cross-functional teams, and supports business development assessments.