- Mount Sinai Hospital (New York, NY)
- …with industry sponsors and CROs. Liaison with CCTO office (including pre- award , post award and QAP). Clinical Research Responsibilities: Responsible for ... with referring and affiliated physicians to ensure documentation of clinical findings throughout the clinical trial...ensure documentation of clinical findings throughout the clinical trial . Collaborates with attending physicians to… more
- Veterans Health Administration (Vancouver, WA)
- …and submit your EDRP application within four months of appointment. Program Approval, award amount (up to $200,000) & eligibility period (one to five years) are ... in written and spoken English. You may be required to serve a trial period. Subject to background/security investigation. Selected applicants will be required to… more
- Hackensack Meridian Health (Edison, NJ)
- …for providing support in the preparation of all financial aspects of grant and clinical trial reporting which include, preparation of budgets for grant / ... clinical trial applications, general ledger grant/...financial responsibilities relating to Research Grant Administration (pre and post - award ). Prepares financial grant reports and invoices… more
- Veterans Health Administration (San Diego, CA)
- …in written and spoken English. You may be required to serve a trial period. Subject to background/security investigation. Selected applicants will be required to ... LMATs who have: Less than one year of experience post licensure; OR, LMATs at the master's level who...as stated on the form. Documentation is required to award preference. For more information on Veterans' Preference, please… more
- Virginia Commonwealth University (Richmond, VA)
- …dystrophies. The Research Administrator will be responsible for providing direct pre and post award support for the Program. The Research Administrator will also ... recipients, preparing RAMS-SPOT submissions, completing sponsor forms, etc. Task 5: Prepare clinical trial budgets and negotiate with sponsors as needed, with… more
- Veterans Health Administration (San Antonio, TX)
- …written instructions. (f) Ability to accurately perform pre-analytical, analytical, and post -analytical phases of testing. Clinical Laboratory Scientist, GS-11 ... and submit your EDRP application within four months of appointment. Program Approval, award amount (up to $200,000) and eligibility period (one to five years) are… more
- University of Utah (Salt Lake City, UT)
- …PRN41958B **Job Title** PS Manager, Clinical Research **Working Title** Clinical Trial & Post Award Manager **Job Grade** G **FLSA Code** ... to ensure continuity and quality of service and care and increase the clinical trial portfolio. Post - award responsibilities include: Facilitate post -… more
- UTMB Health (Galveston, TX)
- …documents needed for Clinical Trials, working in consultation with UTMB Clinical Trial Office. + Develop detailed budgets and justifications that accurately ... submissions. + Prepare required NIH progress reports, working with Department post - award for budgets reconciliation. + Provide document management support,… more
- Beth Israel Lahey Health (Boston, MA)
- …Research Administrator (Research Administrator II)** , provides Pre and Post award support to Joslin investigators for complex Clinical Research awards ... including federal grants and subcontracts, foundation grants and clinical trial agreements. Pre- award responsibilities...faculty and staff on all aspects of pre- and post - award clinical research project proposals… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …science or related field + Certification or evidence of training completed in Clinical Trial Monitoring requirements and best practices REQUIRED SKILLS AND ... EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience in the areas of clinical research and regulatory… more
- Stanford University (Stanford, CA)
- …Clinical Research Financial Management to develop and execute the SCI's clinical trial financial management centralization strategy. Reporting to and ... be responsible for leading and developing a dedicated SCI clinical trial financial management team to oversee...cyclical. + If managing sponsored projects, ability to manage post and pre award administration for sponsored… more
- Mount Sinai Health System (New York, NY)
- …industry sponsors and CROs. + Liaison with CCTO office (including pre- award , post award and QAP). Clinical Research Responsibilities: + Responsible for ... with referring and affiliated physicians to ensure documentation of clinical findings throughout the clinical trial...ensure documentation of clinical findings throughout the clinical trial . + Collaborates with attending physicians… more
- University of Pennsylvania (Philadelphia, PA)
- …monitor treatment, responses to treatment, problems, and adverse events and follow-up. Post - trial responsibilities: case report forms are analyzed, and quality ... ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's...and resources, and much more. Posted Job Title Veterinary Clinical Research Nurse Job Profile Title Veterinary Clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …depending on experience and qualifications. The candidate will help coordinate an NIH funded clinical trial . The NIH study is an investigation of the mechanisms ... ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's...qualifications. The candidate will help coordinate an NIH funded clinical trial . The NIH study is an… more
- University of Pennsylvania (Philadelphia, PA)
- …pre- award activities for diverse clinical research sponsor portfolio. Manage post award activities including account set up, monitor and review of all ... pre- award activities for diverse clinical research sponsor portfolio. Manage post award activities including account set up, monitor and review of all… more
- University of Colorado (Aurora, CO)
- …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial + Perform informed consent process or ensures that ... phone contacts and personal interviews + Schedule subject participation in research clinical trial , coordinating availability of necessary space, and clinical… more
- University of Washington (Seattle, WA)
- …comprehensive and independent review of all documents and data related to the clinical trial funding, including study budget, protocol, contract, and other ... to actual variations and budget development questions. Serve as a resource for clinical trial managers and principal investigators on queries related to the… more
- University of Colorado (Aurora, CO)
- …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial + Perform informed consent process or ensures that ... phone contacts and personal interviews + Schedule subject participation in research clinical trial , coordinating availability of necessary space, and clinical… more
- OhioHealth (Columbus, OH)
- …Grid. Develop comprehensive internal budget including input from various team members for clinical trial budgets by industry as well as investigator initiated ... not limited to cost analysis, calculating potential profit margins, etc. Effectively negotiates clinical trial budgets with study sponsors to ensure all costs… more
- Veterans Affairs, Veterans Health Administration (Brooklyn, NY)
- …and submit your EDRP application within four months of appointment. Program Approval, award amount (up to $200,000) & eligibility period (one to five years) are ... The New York Harbor VA has an opening for a full-time Clinical Psychologist in the Mental Health Residential Rehabilitation Treatment Program. The position… more
