- Actalent (Overland Park, KS)
- Proposal Specialist - Clinical Trials /Government-specific MUST...in-depth EXPERIENCE WITH : + FDA + DOD + NIH + NIDA + BARDA + SAM.gov + GRANTS.gov ... someone (Not Manager Level) to write proposals, write ups, familiar with budgets. NIH and DOD contracts. Three years minimum working on Government Contracts. Typing… more
- University of Washington (Seattle, WA)
- …this position is to manage and administer the grant and financial operations of the Clinical Trials Unit (CTU) in the Division of Cardiology. The CTU is composed ... is required to use independent judgment, strong leadership skills, and knowledge of clinical trial business operations to effectively facilitate work flow and… more
- Johns Hopkins University (Baltimore, MD)
- …and financial management of clinical trials . Classified Title: Clinical Research Program Specialist Job Posting Title (Working Title): Clinical ... research at Johns Hopkins University and across multiple clinical trial sites. This position will serve...trial sites. This position will serve as Lead Specialist for Break Through Cancer (BTC) grant PIs for… more
- Houston Methodist (Houston, TX)
- …IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory compliance. Meets with study monitors. Maintains ... cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- … clinical investigators, laboratory personnel, study sponsors, IRB , Office of Clinical Trials , and support staff. Working knowledge of medical terminology, ... multiple projects at the state and federal levels. The Soc/ Clinical Research Specialist works closely with the...as familiarity with local, state, and federal guidelines governing clinical trials . The candidate must be experienced… more
- Vanderbilt University Medical Center (Nashville, TN)
- …human subjects * Knowledge and understanding of the management and implementation of clinical trial operations * Understanding and capability to perform the ... prior to, during and after the conduct of a clinical trial * Performs packaging and ships...information to ensure only appropriate subjects are enrolled in clinical trials * Participates in the ongoing… more
- Vanderbilt University Medical Center (Nashville, TN)
- …human subjects. + Knowledge and understanding of the management and implementation of clinical trial operations. + Understanding and capability to perform the ... prior to, during and after the conduct of a clinical trial . + Performs packaging and ships...information to ensure only appropriate subjects are enrolled in clinical trials . + Participates in the ongoing… more
- Vanderbilt University Medical Center (Nashville, TN)
- …human subjects + Knowledge and understanding of the management and implementation of clinical trial operations + Understanding and capability to perform the ... information to ensure only appropriate subjects are enrolled in clinical trials + Utilizes nursing skills to...prior to, during and after the conduct of a clinical trial Examine data and records to… more
- National Institutes of Health (Montgomery County, MD)
- …Information Engineering Branch (IEB). Responsibilities As a Supervisory Technical Information Specialist , you will: Serve as a national authority and provide ... of users throughout the world every day and the NIH Manuscript Submission System that supports the NIH...In order to qualify for a Supervisory Technical Information Specialist , GS-1412 position, you must have: A full 4-year… more
- Beth Israel Lahey Health (Boston, MA)
- … supports regulatory compliance for oncology clinical research in the Cancer Clinical Trials Office (CCTO) at Beth Israel Deaconess Medical Center (BIDMC). ... Excel, PowerPoint or Access. **Preferred Qualifications:** + 1-3 years of clinical trial regulatory affairs experience preferred. **Competencies:** **Written… more
- University of Colorado (Aurora, CO)
- …other Federal grants, Federal contracts, State grants, State contracts, private industry clinical trials , association grants and much more. (Principal Level ... Sponsored Project Financial Specialist - 32938 University Staff **Description** **University of...grants, Federal contracts, State grants, State contracts, private industry clinical trials , association grants and much more.… more
- University of Colorado (Aurora, CO)
- …study subject payment forms. + Assist with and oversee the day-to-day operations of clinical trials and studies. + Obtain study subject's medical history and ... criteria, and confirms eligibility of subject to participate in clinical trial . + Perform informed consent process...+ Interview prospective subjects for a variety of research clinical trials . Educate potential subjects on the… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …infection. The laboratory is also designated as an Immunology Specialty Laboratory for the NIH -funded AIDS Clinical Trials Group (ACTG). The candidate will ... of seven National Primate Research Centers funded by the NIH , EPC conducts studies that make breakthrough discoveries possible....from domestic and international cohorts, as well as HIV/AIDS/TB clinical trials samples. The candidate will be… more
- University of Michigan (Ann Arbor, MI)
- …this position. **Summary** The Department of Psychiatry is seeking an experienced Research Specialist to support NIH and VA funded research projects focusing on ... Psych Research Specialist Senior / Intermediate Apply Now **How to...VA hospitals and will be conducted through 2029. The NIH funded study will involve interviews with adults hospitalized… more
- University of Washington (Seattle, WA)
- …applications. * Understand and appropriately utilize multiple sources of income, including clinical trial contracts, federal grants, foundation grants, and gift ... to improve cancer care by moving discoveries made in the laboratory to a clinical setting and finding new and innovative ways to use existing therapies. Our vision… more
- National Institutes of Health (Montgomery County, MD)
- …of drug use and addiction. NIDA supports and conducts basic and clinical research on drug use, its consequences, and the underlying neurobiological, behavioral, ... other graphic assets and to make Institute collections available to internal staff, NIH and DHHS contacts, and the public, as appropriate. Requirements Conditions of… more
- University of Michigan (Ann Arbor, MI)
- …and priorities and may include work on other research studies and behavioral trials across diverse clinical populations (eg, Huntington disease, spinal cord ... Research Area Specialist Inter/Assoc Apply Now **How to Apply** A...follows: last name, first name. **Summary** The Center for Clinical Outcomes Development and Application (CODA) in the Department… more
- Beth Israel Lahey Health (Boston, MA)
- …submit applications, including preparation of consent forms to the IRB on all clinical trials (industry, cooperative groups and PI initiated studies), and ... cooperative group and NCI audits. Coordinate BIDMC participation in audits of clinical trials including internal audits, DFHCC audits, Network institution… more
- Intermountain Health (Provo, UT)
- …spreadsheet applications, and email. Experience using research applications including RedCap, Clinical Trial Management Systems, IRB software, Sales Force, etc. ... **Job Description:** The Research Operations Specialist supports a specific team of research enrollment...study team is following Code of Federal Regulations, Good Clinical Practice, FDA, IRB, NIH , NCI, CAP… more
- Merck (Columbus, OH)
- …Description** The Medical Writing & Disclosure Department of the GCTO (Global Clinical Trial Operations) organization prepares a variety of regulated ... development portfolio and compliance in public disclosure of clinical trials and their results, document disclosure,...Specialist may occasionally prepare plain language (lay) summary trial results at a 6-8th grade reading level and… more