- Emory Healthcare/Emory University (Atlanta, GA)
- …treatments, prevention, community-based research, and laboratory-based translational human immunology. The Clinical Trials Regulatory Specialist I ... 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
- Hackensack Meridian Health (Paramus, 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
- 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
- ThermoFisher Scientific (Wilmington, NC)
- …a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of ... research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver... clinical research services provide end-to-end support for clinical trials from study start up to… 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
- Actalent (Basking Ridge, NJ)
- …and life-enhancing care! Apply Now for more info! Description: + Manages multiple clinical trials . + Oversees reports and assists with statistical analysis. + ... center members. + Builds research infrastructure to support multi-center clinical trials . + Performs project management for...experience in clinical research. + Experience in clinical protocol and trial document development. +… more
- Merck (North Wales, PA)
- …within Fair Market Value based upon protocol design, industry benchmark data and clinical trial team feedback. + Represent Global Site Budgets and Payments ... colleagues while developing and expanding your career. **The Senior Trial Initiation Specialist in Global Site Budgets...on Clinical Trial Teams during trial … 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
- Children's Hospital Boston (Boston, MA)
- …to coordinate and manage clinical research as a part of the Progeria Clinical Trials team at Boston Children's Hospital. The coordinator will interact with ... research subjects and families during complex clinical trial visits and work with our...knowledge of each study. + Maintaining and completing all regulatory documents that include: FDA annual reports, DSMB reports,… 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 ... UPMC Hillman Cancer Center is currently hiring a regular full-time Regulatory Specialist to help support the Oncology Clinical Research Services team located… more
- Hackensack Meridian Health (Paramus, NJ)
- … Practice (GCP), and Institutional policies and procedures as it relates to all regulatory aspects of assigned clinical trials conduct. This role will ... for all regulatory matters concerning all assigned clinical trials and is responsible for the...clinical trial lifecycle for all assigned clinical trials . **Responsibilities** A day in the… more
- National Institutes of Health (Montgomery County, MD)
- Summary If you have experience managing clinical trials and providing regulatory support AND you want to play a significant role in a dynamic organization, ... the following types of tasks: managing a portfolio of clinical trials to include protocol navigation, regulatory support and document preparation; serving… more
- Johns Hopkins University (Baltimore, MD)
- …start-up process and minimize delays. Operational support related to OnCore (JHM Clinical Trial Management System), including the eReg platform, and managing ... Prepare accurate IRB submissions and obtain timely IRB approval. + Submit NDA, clinical trial agreement/contract, and budget approval for review and execution. +… more
- Medtronic (Lafayette, CO)
- … trial design + Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials , such as ISO14155 **About ... consumer application. . Oversees and resolves operational aspects of clinical trials in conjunction with project teams...practice (GCP) and specific country regulations and may prepare clinical trial budgets. . Oversees clinical… more
- Abbott (Abbott Park, IL)
- …(CIP) expertise, to facilitate appropriate trial subject selection for TAVI clinical trials . + Provide procedural guidance to physicians when implanting ... Abbott Structural Heart division. We are seeking an experienced **Field Clinical Specialist (FCS).** Primarily responsibilities will include outstanding… more
- Weill Cornell Medical College (New York, NY)
- …for this role when Hired for NYC Offices **Position Summary** Oversees the clinical trial regulatory maintenance from study submission through closeout. ... Title: Regulatory Specialist Location: Upper East Side...Title: Regulatory Specialist Location: Upper East Side Org Unit: IBD...trials . + Coordinates site visits and audits of clinical trials . + Attends conferences regarding … more
- Banner Health (Greeley, CO)
- …and your future. If you're looking to leverage your abilities - apply today. Cancer clinical trials and research are the basis for virtually all advancement in ... careful study and evaluation of new treatments and therapies, clinical trials help uncover better ways to...aspects of the projects appropriately and adhere to the clinical trial schedule, which may include: maintaining,… more