- 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** : 429 **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
- 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
- RWJBarnabas Health (Belleville, NJ)
- Clinical Informatics Spec I, Onsite, BellevilleReq #:0000155811 Category:Information Systems and IT Status:Full-Time Shift:Day Facility:RWJBarnabas Health ... 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: 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
- University of Rochester (Rochester, NY)
- …quality, safety, efficiency and consistency in the processing of human subject research data . This individual will have responsibility for overseeing ... efficiency and consistency in the processing of human subject research data . Reviews study progress, including ...research -related procedures. + Minimum of 3 years of clinical research or equivalent combination of education… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Coordinates the activities associated with human subject research . This person will be responsible for recruitment and have administrative ... screening and recruiting subjects, performing informed consenting and interviews, completing data entry, and performing medical chart reviews. They will review study… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: With direction from the Clinical Research Manager, assists with coordination of clinical research management activities for large ... international multi-site studies within the Clinical Cardiology Research Center to be consistent...+ Supply and equipment requirements + Extracts and maps clinical data from test data … more
- University of Rochester (Rochester, NY)
- …combination of education and experience required. + Experience as Human Subject Research Coordinator I preferred. + Clinical Skills in phlebotomy, ultrasound ... reports on specific trials, and appropriate close out of clinical trials that are complete. May include travel to...and written communication skills preferred. + Word processing and data analysis software required. + Professional Research … more
- University of Rochester (Rochester, NY)
- …the CTSI Human Subject Research Coordinator Trainee program or other related research experience. + Word processing and data analysis software preferred. + ... GENERAL PURPOSE: Coordinates the activities associated with human subject research . **JOB DUTIES AND RESPONSIBILITIES:** 1. Coordinates the administrative details… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Coordinates the activities associated with human subject research . **RESPONSIBILITIES:** + Coordinates the administrative details required to ... initiate and conduct human subject research , including receiving, distributing and explaining study information, such...and/or any other required recipients or entities. Ensures all data are collected and secured within approved parameters and… more