- Cardinal Health (Jackson, MS)
- **_What Regulatory Submissions Operations contributes to Cardinal Health_** Regulatory Submissions Operations uses specialized technology and knowledge ... 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)
- …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 Project Coordinator II Role/Level/Range: ACRP/04/MC Starting Salary… 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 Project Coordinator Job Posting Title (Working Title):… 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 Project 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 Project 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
- 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 ... projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions . Responsible for representing Quality at business… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …Quality input for Validation projects, clinical studies, stability studies, and Regulatory submissions . Responsible for representing Quality manager at business ... - Monday through Friday: 8:00 am to 5:00 pm ** Sr . Quality Associate I / II / Principal, Quality...Associate I / II / Principal, Quality Assurance:** The Senior Quality Associate I/II/Principal will be assigned duties and… 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)
- …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 Project Coordinator Role/Level/Range: ACRP/03/MB Starting Salary Range:… 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
- Grifols Shared Services North America, Inc (Clayton, NC)
- …Annual Product Reviews as well as providing Quality input for Validation projects, Regulatory submissions and audits. The incumbent will be responsible for ... services in more than 110 countries and regions. **Hours : Day Shift** ** Sr . Quality Associate I:** The incumbent will be assigned duties and responsibilities within… more
- University of Colorado (Aurora, CO)
- …- Requisition: #37493** **Job Summary:** **Key Responsibilities:** + Participates in regulatory submissions for Biological License Applications (BLA), filings, ... **Quality Assurance Coordinator (Entry Senior Level)** **Description** **University...and communications with regulatory and accreditation agencies including audits including but not… more
- Mount Sinai Health System (New York, NY)
- **Job Description** A Senior Clinical Research Coordinator position is available within the Tisch Cancer Institute. The Senior Clinical Research ... Investigator and regulatory staff in the preparation of new protocol submissions , protocol amendments, and renewals of ongoing clinical trials. + Mentors, trains… 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
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior ( Sr .) Regulatory Compliance Specialist position is responsible for leading, coordinating and performing study specific ... regulatory processes such as local IRB submissions ...Procedures (SOPs), and study specific protocols/plans and processes. The Sr Regulatory Compliance Specialist position maintains documentation… more
- Children's Hospital Boston (Boston, MA)
- 81454BRJob Posting Title: Senior Coordinator - Institutional Animal Care & Use Committee IACUCDepartment:Research-Research ... with faculty, postdoctoral fellows and technical staff planning protocol submissions . Reviews science and compares methodology with acceptable institutional 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/OHS policy and patient care requirements...when applicable. **Job Duties** + Coordinates and oversees the regulatory processes as they relate to the evaluation, initiation,… more
- University of Pennsylvania (Philadelphia, PA)
- …includes tracking participants through the timepoints, and assists regulatory submissions as needed. Clinical Research Coordinator B: In addition to ... period and 6 months of service. Job Description Job Responsibilities Clinical Research Coordinator A: Under direct supervision of senior clinical research … more
- HCA Healthcare (Asheville, NC)
- …you want to join an organization that invests in you as a( Physician Recruitment Coordinator ? At HCA, you come first. HCA Healthcare has committed up to $300 million ... (tuition, student loan, certification support, dependent scholarships) + Colleague recognition program + Time Away From Work Program (paid...difference. We are looking for a dedicated Physician Recruitment Coordinator like you to be a part of our… more
- Cedars-Sinai (Los Angeles, CA)
- …**What will I be doing in this role?** In collaboration with the department Senior Vice President and department directors, the Managed Care Coordinator supports ... goals align with broader Health System objectives. The Managed Care Coordinator collaborates with leadership, clinical departments, and external partners to ensure… more