- Stanford University (Stanford, CA)
- Clinical Trials Regulatory Specialist **School of Medicine, Stanford, California, United States** Research Post Date Mar 27, 2024 Requisition # 102688 ... to effect positive changes in patient care. The PACCM is seeking a full-time Clinical Trials Regulatory Specialist (CTRS) to join our expanding … more
- Stanford University (Stanford, CA)
- Clinical Trials Regulatory Specialist 2 **School of Medicine, Stanford, California, United States** Research Post Date Feb 16, 2024 Requisition # 100464 ... innovative clinical research to improve human health. SCCR seeks a mission-driven Clinical Trials Regulatory Specialist 2. You will work with a… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …the diversity and excellence of our academic community. **Description** JOB DESCRIPTION: + The Clinical Trials Regulatory Specialist I is an entry-level ... position supporting regulatory affairs in clinical trial research. + The primary focus... trial portfolio. + Duties include: + Assists regulatory team ( Regulatory Specialist II… more
- Emory Healthcare/Emory University (Decatur, GA)
- …The Regulatory Specialist II is an intermediate level position supporting regulatory affairs in clinical trial research. + Incumbents are responsible ... reports. + Establishes and maintains processes and monitors practices to ensure regulatory documentation involving clinical trials complies with… more
- Methodist Health System (Dallas, TX)
- … clinical , investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, ... requirements * Obtain and facilitate tracking of relevant regulatory documents for clinical trials ...trials assigned. * Assist in the development of clinical trial documents for signature of principal… 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
- Merck (Rahway, NJ)
- …of our pipeline and existing products to produce safe, effective, innovative medicine. The Clinical Trial Specialist partners with the early development ... extend and improve the lives of patients worldwide. Through clinical trials , we ensure the safety and...regulatory requirements + Knowledge of drug development and clinical trial processes, including related standards and… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Senior Associate Director, Clinical Trial Diversity supports the Clinical Development & Operations (CD&O) strategy for Diversity & ... Inclusion in clinical trials , focusing on the US. They...the development and execution of Diversity & Inclusion in clinical trial strategies, core processes and best… more
- Vitalief (New Brunswick, NJ)
- …activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high enrollment, ... Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: +… more
- AbbVie (North Chicago, IL)
- …Job Description Description The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials . They are the primary ... interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes....+ Review of and input into documents related to clinical trial submissions managed by other stakeholders… 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
- University of Colorado (Aurora, CO)
- …Team (CReST) has an opening for a full-time Clinical Research Startup Specialist to provide regulatory and operationalization startup support for a variety ... communicates with these entities in order to operationalize complex clinical trials . + Develops standard operating procedures... Clinical Practice, applicable regulations, and of the clinical trial lifecycle is essential. We are… more
- University of Pennsylvania (Philadelphia, PA)
- …Prepare any necessary regulatory documentation DUTIES: The Clinical Trials , Billing, Budget and Compliance Specialist will report directly to the ... and much more. Posted Job Title Clinical Trials , Billing, Budget and Compliance Specialist Job Profile Title Financial Analyst Job Description Summary Job… more
- Beth Israel Lahey Health (Boston, MA)
- …Type:** Regular **Scheduled Hours:** 40 **Work Shift:** Day (United States of America) The Clinical Trials Specialist II is responsible for fostering and ... to ensure disease groups have appropriate internal organization to effectively comply with regulatory requirements for clinical trials . Serves to provide… 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
- 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)
- …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
- 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
- University of Pennsylvania (Philadelphia, PA)
- …much more. Posted Job Title Clinical Research Coordinator A/B (Infectious Disease Clinical Trials Group) Job Profile Title Clinical Research Coordinator ... Job Description Summary As part of the Infectious Disease Clinical Trials Group, this position will coordinate...include: Assist in development of study documents. Work with Regulatory Specialist for regulatory submissions.… 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