- University of Pennsylvania (Philadelphia, PA)
- …in study team meetings, disease site group meetings, and ongoing protocol training/compliance meetings. Adheres to all University and other regulatory guidelines. ... all data points are collected, 2) Track enrolled study participants throughout the protocol follow up period, offer participants optional follow up procedures per … more
- University of Pennsylvania (Philadelphia, PA)
- …following: screening, recruiting, consenting and enrolling eligible subjects per protocol using GCP guidelines. Scheduling clinical and research visits, interacting ... and inspections. The CRC will participate in study team meetings and ongoing protocol training/compliance meetings and will be expected to adhere to all University… more
- University of Pennsylvania (Philadelphia, PA)
- …history, physical assessments, completion of patient visits according to protocol specifications, administration of investigational products by various routes ... on severity of symptoms and diagnoses, and communicate with medical staff regarding protocol specific management of toxicities and adverse events. In addition to the… more
- University of Pennsylvania (Philadelphia, PA)
- …will oversee 2 or more clinical trial ensuring that the integrity of the protocol is maintained, all data and queries are answered in a timely manner, appropriate ... SAEs are reported to the sponsor and IRB per protocol . The CRC will participate in clinic to explain...will be responsible for gather the data per the protocol and bring any adverse events to the attention… more
- WellSpan Health (York, PA)
- …Assists investigators in evaluating the quality of care and compliance to protocol requirements. Follows by ensuring compliance with all guidelines for human subject ... education to inform clinical and other staff of implications of protocol procedures. Distributes protocol and patient information in a timely manner. + Oversees… more
- University of Pennsylvania (Philadelphia, PA)
- …Disease Program. Screen, recruit, consent and enroll eligible subjects per protocol using GCP guidelines. Implement various research protocols and guidelines. ... events and serious adverse events per protocols. Manage patient treatment per protocol , schedule clinical and research office visits, interact with cardiology and… more
- University of Pennsylvania (Philadelphia, PA)
- …instruct and support investigators and study staff on carrying out clinical protocol and other study related requirements. Job Description This position is ... to assure research activities are conducted with the currently approved protocol /amendments, according to Good Clinical Practice (GCP) guidelines applicable federal… more
- University of Pennsylvania (Philadelphia, PA)
- …conducting study initiation and monitoring visits, and participating in ongoing study protocol training. The CRC is also responsible for research lab specimen ... processing/handling. The CRC will demonstrate vigilance in patient safety, protocol compliance, and data quality, and will participate in data organization for… more
- Parexel (Harrisburg, PA)
- …external stakeholders. The Sr. CRA is responsible for the resolution of all protocol -related issues for assigned investigator sites and will work closely with the ... training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol... protocol and the safeguarding of patients; provide protocol training to, and address protocol related… more
- University of Pennsylvania (Philadelphia, PA)
- …visits and with other divisions and/or service centers as required by the protocol . Arranging transportation to and from study visits + Prepare patient and ... appointments, procedures, or inpatient stays as required by study protocol + Perform specific protocol procedures such...required by study protocol + Perform specific protocol procedures such as interviewing subjects, taking vital signs,… more
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