- University of Pennsylvania (Philadelphia, PA)
- …changes to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies , multi-center research studies ... subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. Assist with Institutional Review… more
- University of Pennsylvania (Philadelphia, PA)
- …coordinate Phase I-IV clinical trials, registries, and other NIH-funded research studies for the Pulmonary Vascular Disease Program. Screen, recruit, consent and ... side effects/adverse events, and maintaining general oversight of patient status throughout study period. Will record and report adverse events and serious adverse… more
- University of Pennsylvania (Philadelphia, PA)
- …preparing trials for audits and inspections. The CRC will participate in study team meetings and ongoing protocol training/compliance meetings and will be expected ... the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing...of the federal regulations for the conduct of clinical studies and human subject protection. + Act in lead… more
- University of Pennsylvania (Philadelphia, PA)
- …Clinical Research Coordinator to organize, coordinate and implement complex cancer studies involving a wide variety of investigational products and various sponsors. ... the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol… more
- University of Pennsylvania (Philadelphia, PA)
- …and (2) meet required obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report directly to the ... (but are not limited to): + Plan, organize, and contribute to study -related meetings, including but not limited to Investigator Meetings, Site Initiation Visits,… more
- University of Pennsylvania (Philadelphia, PA)
- …enrollment, study visits and regulatory compliance in one or more studies . Job Description Research coordinator work includes study implementation, document ... Work directly with investigators to design, set-up and execute studies . Accountable for making sure study timelines...and execute studies . Accountable for making sure study timelines and goals are met. Independently move a… more
- Teleflex (Wayne, PA)
- …site audit, patient safety, electronic data capture and management, and study analysis through publication of scientific publications and regulatory study ... Responsibilities** * Oversees design, implementation, and management of clinical studies with responsibility for quality, timeliness and completeness of execution.… more
- Penn Medicine (Lancaster, PA)
- …Research Associate assists principal investigators in managing and conducting research studies and clinical trials per Federal, State and Institutional guidelines. ... related activities including development of IRB approved research and clinical studies trials site operational management, case coverage and enrollment activities… more
- Pfizer (Collegeville, PA)
- …molecule(s)/indication(s) + Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high ... You will lead and coordinate the development of multiple studies of novel biological and small molecules for first...operations and the project team, to meet enrollment and study delivery timelines. You will also work with other… more
- Geisinger (Danville, PA)
- …Job Duties + Works with principal investigator and research team to implementresearch studies . + Develops and manages study budgets. + Assists in developing ... and adherence, project planning, project tracking and reporting, team management, study finances, data collection and quality, and assisting in the creation… more