Clinical Research Associate Jobs in Pennsylvania, United States

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.

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.

Hematology/Oncology Research team at Rochester Regional Health conducts clinical studies to advance cancer treatments. The Clinical Research Associate supports investigators by preparing study documentation, managing regulatory submissions, enrolling patients, and ensuring compliance with protocols.

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.

Join Thermo Fisher Scientific as a Clinical Research Associate Level II in New York. Conduct remote and on-site monitoring of investigator sites, ensuring protocol compliance, ICH-GCP adherence, and data integrity.

Clinical Research team at Merck conducts ophthalmology trials across the United States. The Senior Clinical Research Associate manages site relationships, ensures protocol compliance, and leads monitoring activities both remotely and on‑site, mentoring junior CRAs.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for rare CNS studies, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations.

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

Senior Clinical Research Associate at IQVIA responsible for monitoring clinical trial sites across multiple U.S. locations. Conducts site visits, ensures compliance with GCP and ICH, manages protocol training, and oversees recruitment, enrollment, and data collection.

The Clinical Research Associate II will oversee oncology clinical trials, ensuring sites follow protocols and regulations. Responsibilities include site visits, data monitoring, and regulatory compliance.

Allegheny Singer Research Institute conducts clinical research and supports investigators. The Research Associate Senior implements and manages technical aspects of R&D projects, plans activities, and liaises between clinical staff and research teams.

Research Associate at Allegheny Singer Research Institute performs laboratory procedures on clinical research specimens, ensuring quality data for physician research. Responsibilities include testing specimens per protocol, operating and calibrating instrumentation, managing quality control records, and handling laboratory animals.

Cornell University College of Veterinary Medicine seeks a Temporary Veterinary Research Associate to support clinical research activities, including data collection, record review, and study coordination. The role involves interpreting veterinary medical records, performing data entry and quality assurance, conducting basic statistical analyses, and providing hands‑on care for cats in clinical trials.

Research Associate - Translational Research at Allegheny Health Network performs routine and complex laboratory procedures on clinical research specimens, mastering laboratory techniques, principles, and instrumentation. Responsibilities include laboratory testing per departmental protocol, independent execution of research tasks, operating and calibrating instrumentation, reviewing quality control and assurance records, caring for laboratory animals, continuing education, and inventory monitoring.

Senior Research Program Coordinator II at GBMC supports principal investigators and research staff across multiple clinical research projects. Responsibilities include regulatory review, site study team training, data monitoring, patient enrollment, and overall project timeline management.

Job Title: Quality Improvement Compliance Monitor Grade: 28 Salary: $109,145 - $117,588 The Research Foundation for Mental Hygiene is seeking a qualified candidate to fill a full-time Quality Improvement Compliance Monitor position. Reporting to the QIE Director and part of the greater HRPP, the incumbent will conduct site initiation visits and post-approval monitoring reviews of human subject research projects to ensure compliance with federal regulations and guidelines and NYSPI policies.

Job Description Summary This is a field-based and remote opportunity supporting key accounts in an assigned geography including, but not limited to, the state of New York and Pennsylvania. Novartis is unable to offer relocation support for this role.

Allegheny Singer Research Institute team coordinates clinical trials, ensuring regulatory compliance and data integrity. The Clinical Research Coordinator Associate assists with data collection, regulatory activities, and patient screening, supporting senior coordinators in trial operations.

Clinical Pathology Research Associate

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.