- University of Rochester (Rochester, NY)
- Clinical Research Data Spec I Next Job Apply for Job When you are ready to apply, registering only takes a minute. Your online account allows you to ... Email this Job **Opening** Full Time 40 hours Range URG 106 EIOH Research Admin Core **Strong Candidate Identified** No job description available **Schedule** 8:30… 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)
- …in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Day-to-day responsibilities include ... studies under the direction of the Principal Investigator and Manager of Clinical Research . Supervision and assistance in training some HSRC-I positions… 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: 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
- 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)
- …has a robust research portfolio that encompasses basic, translational, and clinical research . This individual would support Clinical Trials under ... efficiency and consistency in the processing of human subject research data . + Reviews study progress, including...software, such as ClickIRB and OnCore, needed to manage clinical research . + Assumes personal responsibility for… 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
- 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)
- …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)
- …surveillance studies under the direction of the Principal Investigator and Manager of Clinical Research . This individual will screen and recruit potential study ... candidates, and perform interviews, data and specimen collection, chart...equivalent combination of education and experience preferred. + Certified Clinical Research Coordinator and/or nursing degree preferred.… 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
- University of Rochester (Rochester, NY)
- …CTSI Human Subject Research Coordinator Trainee program or other related research experience required. + Word processing and data analysis software ... 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)
- … Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) ... environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory documents… more