- University of Pennsylvania (Philadelphia, PA)
- …Supports in the monitoring of external sites and assists in the management of multisite trials. Job Description Prepare and process all Institutional Review ... organize and maintain all documentation required by sponsor or CRO (case report forms, source documentation, study and regulatory...in alignment with salary ranges based on external market data for the job's level. Internal organization and peer… more
- Bristol Myers Squibb (Philadelphia, PA)
- …relationships within the medical community + Excellent communication, presentation and time management skills + Translating scientific or clinical data into an ... major evidence read-outs with clinical trial investigators eg, Ph 3 top-line data . + Support Interventional and Non-Interventional Research (NIR) studies ( eg… more
- University of Pennsylvania (Philadelphia, PA)
- …all aspects of clinical trial coordination including subject recruitment, detailed data entry, subject visits, and follow-up and regulatory documentation. The ... for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data… more
- Sumitomo Pharma (Harrisburg, PA)
- …Sourcing/Procurement manager to deliver strategic sourcing, contract management , supplier market intelligence, financial productivity, supplier performance ... organization. The role requires active category knowledge and change management support that challenges traditional spending behavior, service level definition,… more
- University of Pennsylvania (Philadelphia, PA)
- …Organize and maintain all documentation required by the Investigator, sponsor or CRO , includes source documentation, case report forms, and research charts. Collect, ... review and report study data . Complete case report forms and resolve ...and queries with input from a supervisor as required. Management of clinical trials and will need to use… more
- University of Pennsylvania (Philadelphia, PA)
- …Organize and maintain all documentation required by the Investigator, sponsor or CRO , includes source documentation, case report forms, and research charts. Collect, ... review and report study data . Complete case report forms and resolve ...The CRC B will have less supervision in the management of clinical trials and will need to use… more
- Merck (West Point, PA)
- …these interpretations will offer a thorough analysis of clinical pathology data , including correlations to toxicokinetic data , antemortem evaluations, and ... well-written, concise Clinical Pathology reports** that accurately reflect the data collected and the significance/impact on candidate drug development...a clinical pathologist in biotech, pharma or at a CRO is a plus, but not required + Excellent… more
- Charles River Laboratories (Wayne, PA)
- …scheduling, coordination and testing. Also responsible for technical review of generated data and for refinement and development of assays as needed. ESSENTIAL ... DUTIES AND RESPONSIBILITIES: + Assist in the management of on-time delivery of all client projects, eg...activities as necessary. + Provide technical review of generated data . + Oversee/assist with refinement and development of assays… more
- Norstella (Harrisburg, PA)
- …**About Citeline:** Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's ... to regulatory approval, and from product launch to lifecycle management , we provide the intelligence and insight to help...our Clinical Solutions combining platform, services and Real World Data (RWD) offerings to support use cases across the… more
- IQVIA (Wayne, PA)
- IQVIA's Channel and Specialty Data Solutions empower pharmaceutical and MedTech companies with real-time, end-to-end visibility into product movement, inventory, and ... patient access. Through the ValueTrak(R) platform, the team delivers integrated data aggregation, advanced analytics, and customizable reporting to optimize brand… more