- Cardinal Health (Boston, MA)
- …within the discipline of chemistry, manufacturing, and controls (CMC). The _Sr. Coordinator , Regulatory Submissions Operations_ will use specialized ... **_What Regulatory Submissions Operations contributes to Cardinal Health_** Regulatory Submissions Operations provides regulatory affairs and product… more
- Dana-Farber Cancer Institute (Brookline, MA)
- The Clinical Trials Office and the Center for RAS Therapeutics is looking for a Regulatory Coordinator (RC) to provide regulatory support for this new ... groups. of the clinical research project. The RC coordinates aspects of protocol submissions , prepares and submits regulatory documents, and maintains records on… more
- Dana-Farber Cancer Institute (Boston, MA)
- …the Leukemia clinical research project. The RC coordinates aspects of protocol submissions , prepares and submits regulatory documents, and maintains records on ... Trials; protocol and consent design and development and FDA IND and other regulatory required submissions **KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:** + Must… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of study records, and resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to join our program. The GI Oncology Clinical Research Program… more
- Dana-Farber Cancer Institute (Boston, MA)
- …interpretation of clinical research data with lab members. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... A position is immediately available for a Neuropathology Clinical Research Coordinator to join the Precision Medicine Program within the DFCI Department of… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of study records, and resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... all of those affected by cancer. The Clinical Research Coordinator II (CRC II) will be an integral part...samples to external entities as necessary. Responsible for maintaining regulatory binders and assuring study compliance with all state,… more
- Boston University (Boston, MA)
- …adverse event reports, deviations reporting, data collection and adherence to current regulatory good clinical practices (GCP) guidelines. Also, coordinator will ... **RESEARCH COORDINATOR , School of Medicine, Surgery** **Job Description** **RESEARCH...Board (IRB) and Biosafety Committee (IBC) medical writing and submissions for study applications, informed consent forms (ICFs) and… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …of study records, and resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... **This Clinical Research Coordinator will be responsible for helping to coordinate...of protocols through the Scientific Review Committee and IRB submissions , and site activation activities. + Responsible for data… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of study records, and resolution of data queries. + Prepare and/or complete regulatory related reports and IRB submissions . Maintain and organize study databases ... Early Detection and Interception of Blood Cancers seeks a **Clinical Research Coordinator ** to assist in the day-to-day management of non-interventional trials. This… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …of study records, and resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and… more
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