- Amerant Bank (Pinecrest, FL)
- …but not limited to deposits, withdrawals, check cashing, issuance of cashiers' checks. Research and resolve issues related to end of day banking center balancing.May ... inquiries. Follow Bank policies and procedures, as well as legal and regulatory requirements, including security and audit procedures.Adhere to all policies and… more
- Merck & Co. (Durham, NC)
- …(QNs), and other key automation-related processesProviding direct support for regulatory inspections and audits and other validation activities by serving ... Production Fermentors and supporting tanks, supporting YSI, Raman, and Mass Spec equipment, supporting Bulk Chemical equipment, implementations of process change… 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 ... the Principal Investigator (PI) and other study team members, the Clinical Research Regulatory Coordinator I exhibits increased learned skills and flexibility… more
- University of Rochester (Rochester, NY)
- …human subject research data + Ensures compliance with all applicable regulatory and institutional requirements and standards. + Maintains regulatory records ... GENERAL PURPOSE: Human Subject Research Specialist II is a mid-level clinical ...maintaining study participant safety and adherence to approved protocols, regulatory guidelines and operational procedures. **JOB DUTIES AND RESPONSIBILITIES:**… more
- University of Rochester (Rochester, NY)
- …communities and reduce barriers to participation. + Provide guidance on research methodologies, regulatory requirements, and ethical considerations, fostering ... adult populations. **Other** **:** + Maintains current working knowledge of clinical research best practices, updates to federal regulatory , Good Clinical… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Under the direction of the Research Manager, with latitude for independent judgement, this individual will have the responsibility for managing ... clinical research trials, from industry, NIH, foundations and internal funds....human recruitment, enrollment, and follow-up of volunteers while meeting regulatory , University and sponsor requirements for the projects. Other… more
- University of Rochester (Rochester, NY)
- …Supports the contacts and relationships between and among Principal Investigator (PI), research staff, study sites and sponsoring and regulatory agencies. ... safety, efficiency and consistency in the processing of human subject research data. This individual will have responsibility for overseeing administrative processes… more
- University of Rochester (Rochester, NY)
- …The individual in this role will monitor and maximize adherence to research standards, regulatory guidelines, and approved operational procedures; work closely ... GENERAL PURPOSE: This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and… 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 ... and document adverse events as advised by the Principal Investigator, and ensure regulatory and other documents (such as consent forms and CRFs) are complete,… 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 ultimate responsibility of the Principal… more
- University of Rochester (Rochester, NY)
- …enroll research subjects for clinical study. Ensures compliance with regulatory and institutional requirements/standards. + Assist in Preparing and submitting ... GENERAL PURPOSE: Serves as a research coordinator of a NIH funded grant, UPSIDE...virtual visits per protocol. Ensures compliance with study protocol, regulatory and institutional requirements/standards. **RESPONSIBILITIES:** + Ensure integrity of… more
- University of Rochester (Rochester, NY)
- …staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, ... clinical trial office staff, and sponsor-designated contacts (eg, Clinical Research Associates (CRAs)) to resolve data inquiries as needed. Responsible… more
- Medtronic (North Haven, CT)
- …that Change Lives** In this exciting role as a **Senior Clinical Research Specialist** (CRS) in our **Robotic Surgical Technologies** Business Unit, you will ... BDM, Safety, EDC. . Trains study sites, ensures site compliance in regulatory requirements, maintains follow-up compliance, and represents Medtronic as a prime… more
- University of Rochester (Rochester, NY)
- …Interface with study monitors to answer any questions and keep complete regulatory and subject documentation. ** Research Team Collaboration (10%):** 5% ... full-time position (40 hrs/wk) in Ob/Gyn to conduct clinical research studies. In particular this individual will be responsible...PI, the sponsor, and the data monitors to ensure regulatory and other documents are complete and on time.… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Coordinates the activities associated with human subject research . **JOB DUTIES AND RESPONSIBILITIES:** 1. Coordinates the administrative details ... required to initiate and conduct human subject research , including receiving, distributing and explaining study information, such...adverse events as advised by the PI and ensures regulatory and other documents, such as consent forms and… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: Coordinates the activities associated with human subject research and data management for geriatric oncology clinical research activities and ... the administrative details required to initiate and conduct human subject research , such as, receiving, distributing, and explaining study information, including… 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...adverse events as advised by the PI and ensures regulatory and other documents, such as consent forms and… more
- Sharp HealthCare (Santee, CA)
- …and anticipated outcomes.Courtesy and customer service will be measured by PT Spec III or Supervisor observation, physician and peer feedback, SharpStar nominations ... meets all third-payer (Medicare, PPO, Work Comp and HMO) and regulatory requirements.Completes notes and TouchWorks billing to meet billing requirements… more
- UTMB Health (Galveston, TX)
- Quality & Patient Safety Spec - Quality Management **Galveston, Texas, United States** Nursing & Care Management UTMB Health Requisition # 2401004 **JOB SUMMARY:** ... and maintain Quality and Patient Safety standards of care provided to patients. Research , collect and analyze internal and external data for decision making. Serve… more
- Covenant Health Inc. (Morristown, TN)
- …conjunction with the Stroke Medical Director, Stroke Nurse Practitioner, Regulatory , Quality, and Hospital Administration to maintain Primary Stroke Certification. ... Stroke Program. Submits required data to the Joint Commission and other regulatory agencies as requested. + Examples: patient satisfaction, discharge phone calls,… more
