Clinical Research Associate Jobs in Pennsylvania, United States

The In-House Clinical Research Associate at Ocugen supports the planning, execution, and closeout of clinical studies to ensure quality, timelines, and regulatory compliance. Day-to-day work includes study start-up and maintenance, TMF/eTMF document control and QC, CTMS data tracking, vendor and site coordination, and supporting CRAs and CTMs with operational and inspection-readiness tasks.

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.

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.

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.

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.

The Clinical Research Associate (CRA) is responsible for monitoring and supporting clinical study sites to ensure the rights, safety, and well-being of study participants and the integrity of clinical data. The CRA conducts site qualification, initiation, interim monitoring, and closeout activities in accordance with study protocols, applicable regulations, Good Clinical Practice (GCP), and company standard operating procedures (SOPs).

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Job Overview Provide strategic quality leadership and oversight across assigned Quality Assurance (QA) programs, with a strong focus on clinical research, clinical operations, pharmaceutical development, and GxP-regulated activities. Influence quality outcomes across multiple functional areas, business units, and customer engagements through expert guidance, risk-based decision making, and oversight of quality systems and compliance programs.

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

IQVIA Biotech is expanding its Clinical Monitoring team and seeks CRA 2 professionals to ensure the successful execution of clinical trials for biotech sponsors. In this role, you will monitor and manage clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations, directly contributing to the integrity and quality of clinical research data.

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.

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.

Oncology Clinical Development – Hematology team drives the design and execution of clinical research for new and marketed oncology medicines. The Senior Clinical Director leads end‑to‑end clinical development, overseeing trial design, regulatory strategy, data analysis, and cross‑functional collaboration.

Allegheny Health Network Clinical Research team coordinates and manages hematologic oncology trials, ensuring patient safety and regulatory compliance. The coordinator identifies eligible patients, educates them and families, collects and maintains trial data, and oversees all trial activities from initiation to completion.

The Clinical Trial Research Monitor at Penn State College of Medicine will oversee clinical trial monitoring for the Beat Childhood Cancer Research Consortium (BCC), a CRO with 50+ hospitals across US and Canada. Responsibilities include ensuring participant rights, data accuracy, and compliance with ICH GCP, local and global regulations, and BCC SOPs.

Clinical Research Interns at the Penn State College of Medicine’s Clinical Trials Office will support the design, execution, and monitoring of clinical studies. They will recruit and schedule participants, obtain informed consent, maintain databases, and assist with protocol compliance and adverse event reporting.