- University of Pennsylvania (Philadelphia, PA)
- …aspects of clinical trial coordination including subject recruitment, detailed data entry, subject visits, and follow-up and regulatory documentation. The ... University of Pennsylvania, Penn Medicine, FDA, GCP and other regulatory standards. The Clinical Research Coordinator (CRC)...with sponsors and/or CROs. + Show vigilance in patient safety , protocol compliance, and data quality. +… more
- University of Pennsylvania (Philadelphia, PA)
- …responsible for accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and ... specimen processing/handling. The CRC will demonstrate vigilance in patient safety , protocol compliance, and data quality, and...of study related activities including but not limited to regulatory submissions, data entry, and regulatory… more
- Bausch + Lomb (Harrisburg, PA)
- …clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance, and clinical data management. + ... departments (eg, R&D/Project Management, Clinical /Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/Device Safety… more
- Merck (West Point, PA)
- …Not Indicated **Valid Driving License:** No **Hazardous Material(s):** n/a **Required Skills:** Clinical Data Interpretation, Clinical Judgment, Clinical ... **Job Description** **Principal Scientist (R5), Clinical Pathology, Pathology, Non- clinical Drug Safety , West Point** Our company is a leading global… more
- Merck (North Wales, PA)
- …clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be ... and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study… more
- University of Pennsylvania (Philadelphia, PA)
- …visits and regulatory compliance in one or more studies. Duties: Clinical ResearchCoordinator B: Participate in and coordinate clinical trials within the ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Division of Infectious Diseases) Job...forms and source document tools. Show vigilance in patient safety , protocol compliance and data qualify. Adhere… more
- University of Pennsylvania (Philadelphia, PA)
- …systems, assessment of adverse events. This coordinator will assist in ensuring patient and data safety , manage samples and related processing, and will be a ... course of the study. + Creates and maintains research data , regulatory files, subject data ...studies and determine patient eligibility by communicating with physicians, clinical staff, and by reviewing medical data .… more
- University of Pennsylvania (Philadelphia, PA)
- …institutions to ensure high-quality execution of research protocols. Attention to patient safety , data integrity, and regulatory compliance is essential. ... and storage of biological samples and related study documents, and collection of clinical data . Assist with Institutional Review Board (IRB) filings and… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …Lectures at national and international meetings, scientific advisory board meetings, and data safety monitoring boards. + Mentors junior team members. ... to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The...potential for meeting an unmet medical need, establishing early clinical safety and proof of concept, conduct… more
- Teleflex (Wayne, PA)
- … Data Management Groups, Core Imaging and Biometric Laboratories, Biostatisticians, Data Safety and Monitoring committees, Event Adjudication committees, etc. ... Senior Director, Clinical Evidence Generation (REMOTE) **Date:** Jul 23, 2025...and management, consent and IRB interactions, site audit, patient safety , electronic data capture and management, and… more