- Johns Hopkins University (Baltimore, MD)
- …development and preparation of regulatory documents as appropriate. + Applies knowledge of study design to evaluate new protocols. + Applies knowledge of federal & ... required for assigned trials. + Oversees & collaborates in development of study tools including data collection forms, eligibility checklists, preprinted orders, &… more
- Takeda Pharmaceuticals (Boston, MA)
- …and UAT scripts based on business requirements and technical specifications to verify study /library functionality in EDC system and adherence to standards. + Drive ... study database user acceptance testing activities in a role...of other data deliverables. + Lead UAT activities for studies and libraries in EDC system, including inbound integrations… more
- Cedars-Sinai (Los Angeles, CA)
- …and leading staff. + Provides guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies . + May assist ... III is responsible for all activities associated with clinical study coordination, subject enrollment, data management/integrity, regulatory compliance, project/… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Detection & Interception clinical research program and lead recruitment for our research studies on the Longwood campus. This role will support the research team in ... and consenting efforts at the Longwood campus, providing timely entry of study data into clinical trials management software, screening for protocol eligibility, and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …submissions, prepares and submits regulatory documents, and maintains records on assigned studies to ensure regulatory compliance with DFCI and DF/HCC policies as ... with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials… more
- University of Pennsylvania (Philadelphia, PA)
- …and external groups. Work directly with investigators to design, set-up and execute studies . Accountable for making sure study timelines and goals are met. ... disease states and varying complexities. Research coordinator work includes study design, protocol development, submission to review boards, subject recruitment… more
- Stanford University (Stanford, CA)
- …managing research projects. The CRC2 will be instrumental in overseeing research studies primarily focused on pain and pain management in the perioperative period. ... individualized way. We conduct longitudinal, perioperative observational and interventional studies in surgical and chronic pain patients. Interventions range from… more
- University of Colorado (Aurora, CO)
- …efforts, as well as data collection on a large scale longitudinal cohort study and innovative clinical trial. These studies utilizes innovative data collection ... This position reports to the Project Director. Because these studies involve families, all visits will need to occur...Data Collection and Management_** + _Lead efforts to retain study participants over the course of study … more
- Genentech (South San Francisco, CA)
- …data & insights, and AI/ML solutions. It spans hypothesis and study design (protocol authoring, approvals, ELN linkage), experiment orchestration (intake, ... research to deliver a coherent, end-to-end product experience spanning across various study designs. Your mandate is to translate scientific strategy into an… more
- Air National Guard Units (Flowood, MS)
- …education and competencies necessary for successful job performance such as, studies in the Sociology, Psychology, Social Welfare, Education, or Human Resources. ... Successful completion of a full four-year course of study in an accredited college or university that resulted...work may serve as a prerequisite for more advanced studies in the field or subject-matter area. Related course… more