- Cedars-Sinai (Los Angeles, CA)
- …the Los Angeles that need our care the most. **Req ID** : HRC1444436 **Working Title** : Clinical Research Data Spec . I - Smidt Heart Institute (Ouyang ... bioinformaticians focused on high impact cardiovascular clinical research . As a Clinical Research Data Specialist I, you will manage the data for… more
- Cedars-Sinai (Los Angeles, CA)
- …Los Angeles that need our care the most. **Req ID** : HRC1338274A **Working Title** : Clinical Research Data Spec III - Smidt Heart Institute ... organization known nationally for excellence in research !** **JOB SUMMARY:** The Clinical Research Data Specialist III manages the data for assigned… more
- Cedars-Sinai (Los Angeles, CA)
- …the Los Angeles that need our care the most. **Req ID** : HRC1365483A **Working Title** : Clinical Research Data Spec I - Smidt Heart Institute (Dr. ... skills with an organization known nationally for excellence in research !** The Clinical Research Data Specialist I manages the data for assigned … more
- University of Rochester (Rochester, NY)
- …AND RESPONSIBILITIES:** + Logs in and performs thorough review of high-volume incoming research data for multiple studies for accuracy and completeness, and ... and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed… more
- University of Rochester (Rochester, NY)
- …considerations, fostering the professional development of trainees in clinical research . **Maintains oversight of study data for the assigned projects:** ... We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic...regularly for conformity with standard operating procedures and verify data to ensure compliance with requirements of the protocol,… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, ... coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the...documents and research records. + Accurately enters research data into data collection… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and ... evaluating multiple clinical research protocols. Under the ultimate responsibility...as consent forms, letters, and appointment notices. + Collect clinical data during all phases of care… more
- Tufts Medicine (Boston, MA)
- …of Value and Risk in Health (CEVR), **which is part of the Institute for Clinical Research and Health Policy Studies at Tufts Medical Center in Boston.** The ... analysis. The position will involve close collaboration with the SPEC research team. The Database Coordinator will...obtain health plan specialty therapy coverage policies 3. Perform data quality control checks 4. Support research … more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Under the direction of the senior staff, the Clinical Research Data Specialist II (CRDS II) exhibits increased learned skills and ... flexibility in performing duties, and assumes responsibility for the data management of clinical research protocols. With minimal supervision, and latitude… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Data Specialist II at the URCC NCORP Research Base Clinical Trials Network and Program is responsible for ... queries; and ensuring complete, accurate, high-quality datasets for analysis. The Clinical Research Data Specialist II also assists with oversight of… more
- Vanderbilt University Medical Center (Nashville, TN)
- … research protocols with some guidance. Ensures the integrity and quality of clinical research is maintained. . KEY RESPONSIBILITIES * Inputs, reviews and ... data lock, monitoring and audit deadlines for multiple studies. * Queries research team to clarify, reconcile and complete data issues. Identifies and… more
- Tufts Medicine (Boston, MA)
- …of Value and Risk in Health (CEVR), **which is part of the Institute for Clinical Research and Health Policy Studies at Tufts Medical Center in Boston.** The ... cost-effectiveness analyses. Activities include but are not limited to data extraction, management and analysis, review and summary of...area of study. 2. Three (3) years of academic, clinical , or scientific research in a medical… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as a Research Scientific Associate Director, Mass Spec in our Cambridge, MA location. _Objective ... develop/transfer assays, oversee data generation/analysis and delivery of high-quality data from global clinical trials under regulated settings (GLP, GCP,… more
- RWJBarnabas Health (West Orange, NJ)
- Clinical Informatics Spec IV, HybridReq #:0000156189 Category:Information Systems and IT Status:Full-Time Shift:Day Facility:RWJBarnabas Health Corporate ... and analytical sciences to identify, define, manage, and communicate data , information, knowledge, and wisdom in clinical ...health. They will lead, design and execute on new research / initiatives and/or analyze data for new… more
- RWJBarnabas Health (Belleville, NJ)
- Clinical Informatics Spec I, Onsite, CMMC - Belleville, NJReq #:0000155811 Category:Information Systems and IT Status:Full-Time Shift:Day Facility:RWJBarnabas ... information management and analytical sciences to identify, define, manage, and communicate data , information, knowledge, and wisdom in clinical practice. The … more
- University of Rochester (Rochester, NY)
- …for independent judgement, this individual will have the responsibility for managing clinical research trials, from industry, NIH, foundations and internal ... will oversee the day to day operations of the clinical research , support personnel as well as...serious adverse event reports. + Using knowledge of Good Clinical Practice standards, maintains data on patients… more
- University of Rochester (Rochester, NY)
- …PURPOSE: Human Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated with ... for the particular study. This role will assume responsibility for less complex clinical research protocols, receiving guidance and instruction from senior level… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Regulatory Coordinator I is an entry level position, responsible, under close supervision, for the coordination and ... oversight of regulatory requirements of clinical research protocols. Under the direction of...and/or infection control standards preferred. + Understands and follows data integrity standards and processes preferred. + Strong interpersonal,… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Human Subject Research Specialist II is a mid-level clinical research coordinator responsible for assisting in the planning, coordinating, ... documents and research records. + Accurately enters research data into data collection...in UR-specific research software needed to manage clinical research protocols Other duties as assigned… more
- University of Rochester (Rochester, NY)
- …for purposes of clinical research and quality improvement + Capture clinical and other performance or management data from several systems to create this ... transcribed from each of these patient charts into electronic data capture systems which consists of clinical ,...the IRB status of submitted projects, to support the clinical research team in conducting ethical … more