- Cardinal Health (Boise, ID)
- …committed to making a difference for our customers and communities. **_What Regulatory Submissions Operations contributes to Cardinal Health_** Regulatory ... and compile paper and electronic documents related to the pharmaceutical industry regulatory submissions throughout each phase of drug development and though… more
- Johns Hopkins University (Baltimore, MD)
- …experience. **Preferred Qualifications** + Related Master's Degree. Classified Title: Sr . Research Program Coordinator II Role/Level/Range: ACRP/04/MC Starting ... the Clinical Research Program Manager, we are seeking a **_Sr. Research Program Coordinator II who_** will be responsible for study site activation and management,… more
- Johns Hopkins University (Baltimore, MD)
- …research staff in complying with protocol requirements. + Prepare initial protocol submissions , develop consent forms and other regulatory documents in ... cash disbursement and reconciliation experience. + Experience using REDCap. Classified Title: Sr . Research Program Coordinator Job Posting Title (Working Title):… more
- Johns Hopkins University (Baltimore, MD)
- …locations within multi-centered clinical trial. + Develop standard operating procedures for regulatory submissions as needed. + Maintain a continued high level ... of research methodology and working knowledge of computers. Classified Title: Sr . Research Program Coordinator II Role/Level/Range: ACRP/04/MC Starting Salary… more
- Johns Hopkins University (Baltimore, MD)
- …studies under the Artificial Intelligence and Technology Collaboratory (AITC). The Sr . Research Program Coordinator will provide administrative and reporting ... Experience with online data collection interfaces (eg, REDCap). Classified Title: Sr . Research Program Coordinator Role/Level/Range: ACRP/03/MB Starting Salary… more
- Johns Hopkins University (Baltimore, MD)
- The Department of Neurology is seeking a ** Sr .** **_Research Program Coordinator , Language Neuromodulation Lab_** for NIH-funded projects on the effects of ... experience with patients with aphasia is highly desired. Classified Title: Sr . Research Program Coordinator Role/Level/Range: ACRP/03/MB Starting Salary Range:… more
- Johns Hopkins University (Baltimore, MD)
- …Hopkins IRB procedures and human subjects research compliance. Classified Title: Sr . Research Program Coordinator Role/Level/Range: ACRP/03/MB Starting Salary ... on suicide prevention, psychological autopsy, and lethal means (firearms) access. The coordinator will work closely with Dr. Paul Nestadt and an interdisciplinary… more
- Johns Hopkins University (Baltimore, MD)
- …as required including recruitment, data collection, biospecimen shipping and tracking, regulatory submissions and site coordination and training for multi-center ... to the extent permitted by the JHU equivalency formula. Classified Title: Sr . Research Program Coordinator Role/Level/Range: ACRP/03/MB Starting Salary Range:… more
- University of Miami (Miami, FL)
- …University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Sr . Regulatory Analyst to work at the UHealth Medical Campus in Miami, ... FL. The Sr . Regulatory Analyst will be responsible for...audit response commitments and work with the CAPA lead coordinator . + Attend PSG meetings to provide regulatory… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions . Responsible for representing Quality at business ... of domestic (ie Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines. **Education and Experience:** Sr . Quality… more
- Johns Hopkins University (Baltimore, MD)
- …for IRB such as Change in Research applications, Continuing Review or other Regulatory submissions when needed. + Prepares for and participates in monitoring ... to the extent permitted by the JHU equivalency formula. Classified Title: Sr . Research Program Coordinator Role/Level/Range: ACRP/03/MB Starting Salary Range:… more
- University of Rochester (Rochester, NY)
- …the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE: The Sr . Clinical Trials Project Mgr. role supports the URCC NCORP ... culture. + Monitor compliance with program guidelines, deadlines, and regulatory requirements, ensuring accountability across the Research Base. + Work… more
- Johns Hopkins University (Baltimore, MD)
- …consent forms, as appropriate. + Collaborates in development and preparation of regulatory documents as appropriate. + Applies knowledge of study design to evaluate ... for review & input as appropriate. + Assures compliance with local & national regulatory standards. + Collaborates with study team and pharmacy to prepare drug data… more
- First Student (Cincinnati, OH)
- …advanced training and technology the transportation industry has to offer.** The Sr . Retirement Analyst works both independently and in a team setting supporting ... on employee issues and requests with timely resolution. The focus of the Sr . Retirement Analyst role is compliance and more complex issue resolution. Higher-level… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …**Description** The Emory Office of Continuing Medical Education (CME) is seeking a Senior Program Coordinator to join the team! Under the direction of ... the associate director, the Sr . Program Coordinator will oversee operations, meeting...users regarding LMS logins, credit claiming, password resets, disclosure submissions , compliance questions, and troubleshooting issues. + Organize and… more
- Ochsner Health (New Orleans, LA)
- …and participating in clinical trials. Independently organizes and manages all documentation and regulatory submissions as required by the sponsor of the trial, ... regulatory agencies, research division/ Occupational Health and Safety (OHS)...of Clinical Research Associates (SOCRA) or Certified Clinical Research Coordinator (CCRC) certification by the Association of Clinical Research… more
- Texas A&M University System (Bryan, TX)
- Job Title Senior Administrative Coordinator I Agency Texas A&M University Health Science Center Department College Of Nursing Proposed Minimum Salary ... care delivery. What we want Join our team the Texas A&M College of Nursing as a Senior Administrative Coordinator I! In this role, you will serve as Senior … more
- Vitalief (New Brunswick, NJ)
- …Coordinator , with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, IRB submissions , data management ... that ultimately benefit patients. We are seeking several problem-solving, enthusiastic Senior Clinical Research Coordinators (as full time, fully benefited Vitalief… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of study records, and resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... in the clinical trial setting and identifying potential targets for intervention. The Senior CRC supports the research team in the overall conduct of clinical trials… more
- Novant Health (Winston Salem, NC)
- …requirements related to the conduct of research (FDA, GCP, IRB, ICH). Assures regulatory submissions for all protocols, adverse events, revisions, renewals, and ... to join our Clinical Research team! The Clinical Research Coordinator (CRC) is a professional working under the direction...study sponsors. Arranges and attends monitoring visits. Works with Sr . team members to prepare for and attend sponsor… more