- University of Pennsylvania (Philadelphia, PA)
- …as assigned. Job Description + Clinical Research Regulatory Affairs Specialist A Assist in Clinical Trial proposal submissions. Provides day-to-day ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist A...provide regulatory support and expertise associated with clinical trials . The person will support a… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist B Job Description Summary The...regulatory aspects of the initiation of Phase I-V clinical trials with a focus on required… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …can contribute to the diversity and excellence of our academic community. **Description** The Clinical Trials Regulatory Specialist I is an entry-level ... position supporting regulatory affairs in clinical trial research. The primary focus of...small trial portfolio. KEY RESPONSIBILITIES: + Assists regulatory team ( Regulatory Specialist II… more
- University of Southern California (Los Angeles, CA)
- … SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -Research- Regulatory - Specialist ... information pertinent to studying milestone progress, including but not limited to: clinical trial management systems, IRB databases, internal and external… more
- University of Pennsylvania (Philadelphia, PA)
- …Title Veeva Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical Research Regulatory Specialist B Job Description Summary The ... is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and...CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to… more
- Houston Methodist (Houston, TX)
- …event reports, safety reports, and notifies IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory ... and study specific protocols/plans and processes. The Regulatory Compliance Specialist position maintains documentation for clinical research studies, case… more
- Hackensack Meridian Health (Edison, NJ)
- …Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant… more
- HonorHealth (Phoenix, AZ)
- …and familiarity with basic finance and accounting principles. The successful Associate Clinical Trials Operations Specialist will support business activities ... in contract or budget terms. The tasks the Associate Clinical Trial Operations Specialist must...closely with Principal Investigators, Clinical Program Leads, Regulatory , Finance, Clinical Trials Personnel,… more
- Actalent (New Brunswick, NJ)
- Job Title: Clinical Trial Specialist Job Description As a Clinical Trial Specialist , you will be integral to the protocol activation process, ... ensuring the initiation and activation of new clinical trial protocols. This includes the preparation and review of study tools, verification of approvals, and… more
- Actalent (New Brunswick, NJ)
- Job Title: Clinical Trial Specialist + As a Clinical Trial Specialist , you will be integral to the initiation, activation, and ongoing management ... of clinical trials . + You will collaborate with...and performance, while staying current with continuing education and regulatory requirements. Hard Skills + 2-3 years clinical… more
- UCLA Health (Santa Monica, CA)
- Description The Division of Hematology-Oncology is seeking an experienced Senior Clinical Trial Specialist to join our team. In this role you will be ... the liaison for the site management and monitoring of clinical trials in Santa Monica. Responsible for...conduct Site Initiation Visits and Interim Monitoring Visits with clinical trial sponsor representatives; you will also… more
- Rush University Medical Center (Chicago, IL)
- …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents in order to ... PM) **Summary:** This position will create coverage analyses in accordance with Medicare's Clinical Trial Policy (NCD 310.1) and assist research staff within the… more
- Rush University Medical Center (Chicago, IL)
- …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents to prepare a ... - 4:30:00 PM) **Summary:** Reporting to the Director/Manager of Clinical Trials Research Revenue Cycle, this position...position will create coverage analyses in accordance with Medicare's Clinical Trial Policy (NCD 310.1) and assist… more
- Rockefeller University (New York, NY)
- …see the hospital website at: http://www.rucares.org/ Overview The Clinical Research Specialist serves as a regulatory expert and resource for investigators ... and new investigator audits, tracks deviations for early intervention, and supports clinical trial registration in Good Clinical Practice (GCP)… more
- Rush University Medical Center (Chicago, IL)
- …activities. Responsible for managing, reconciling and invoicing all revenue secured by Clinical Trials Research Revenue Cycle, work closely with operations, ... requirements specific to Research Billing. * Maintain a detailed understanding of Medicare's Clinical Trial Policy (NCD 310.1) and related guidance documents. *… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The responsibility of the Clinical Trials Project Specialist IA is to help coordinate all aspects of multi-center international clinical ... This position assists more senior team members in supporting clinical trial sites. Responsible for helping prepare...equivalent combination of education and experience required + Some clinical trials experience preferred + Knowledge of… more
- Dignity Health (Phoenix, AZ)
- …Manages the daily operation and supervision of the Clinical Research Regulatory Affairs area and program specialist (s) in accordance with all applicable ... initiation and monitoring visits performed by pharmaceutical and device manufacturing clinical trial sponsors. Responsibilities Include: + Manages all functions… more
- ThermoFisher Scientific (Morrisville, NC)
- …and proactive escalation. **Qualifications:** **Education and Experience:** + Experience with Clinical Trial (Phase 1-4) preferred + Previous experience in ... and Abilities:** + Strong knowledge of budgeting and forecasting + Good knowledge of Clinical Trials + Excellent leadership skills + Strong attention to detail… more
- Dana-Farber Cancer Institute (Boston, MA)
- …including live teaching and development of educational materials. The CNE assists the Clinical Specialist policy owners with the development of policy and ... clinical instruction to staff for competency development 9. Coordinates with Director, Clinical Specialist , CCPD, and Preceptors to provide orientation to new… more
- UPMC (Pittsburgh, PA)
- …regulatory portion of the trial submission process, and to maintain the regulatory integrity of assigned clinical trials from approval to closure ... Hillman Cancer Center is currently hiring a regular full-time ** Regulatory Specialist ** to help support the Oncology Clinical Research Services team located… more