- Mayo Clinic (Rochester, MN)
- …through the clinical trial development/implementation process; writing of the informed consent document; coordination of study logistics/approvals, verification ... tools and technology. Knowledgeable with reg docs, IRB submission, writing consent forms. **Exemption Status** Exempt **Compensation Detail** $64,500.80 - $96,824.00… more
- HCA Healthcare (Austin, TX)
- …role:** Prepare patients for diagnostic stress tests, including interviewing, obtaining informed consent , skin preparation for electrode placement, obtaining ... and inclusion thrive? Submit your application for our Exercise Specialist opening with Austin Heart today and find out...a healthier tomorrow."- Jane Englebright, PhD, RN CENP, FAAN Senior Vice President and Chief Nursing Executive If you… more
- Vanderbilt University Medical Center (Nashville, TN)
- …appropriate subjects are enrolled in clinical trials. + Participates in the ongoing informed consent process, ensuring that human subjects, their families, and ... Under the guidance and supervision of the Principal Investigator, the Research Nurse Specialist II (RNS II) is responsible for assuring that the integrity and… more
- Vanderbilt University Medical Center (Nashville, TN)
- …appropriate subjects are enrolled in clinical trials * Participates in the ongoing informed consent process, ensuring that human subjects, their families, and ... Under the guidance and supervision of the Principal Investigator, the Research Nurse Specialist II (RNS II) is responsible for assuring that the integrity and… more
- Sanford Health (Sioux Falls, SD)
- …in subject medical records to confirm study eligibility. Review study protocol, informed consent form and follow-up procedures with potential study subjects. ... logs and appropriately update sponsors, contract research organizations (CROs) and/or senior medical officers (SMOs). Assure the completion of all screening,… more
- Ascension Health (Lisle, IL)
- …are consistent with approved proposals to open new studies. Reviews and modifies Informed Consent documents to reflect the Ascension Illinois mission. Attends ... and 2,600 sites of care, including more than 140 hospitals and 40 senior living communities in 19 states. Our Mission, Vision and Values encompass everything… more
- GE HealthCare (Boston, MA)
- …to verify compliance with GCP standards. This involves reviewing study protocols, informed consent forms, case report forms, regulatory submissions, and other ... **Job Description Summary** The Good Clinical Practice (GCP) Senior Quality Assurance (QA) Auditor is crucial in...not limited to CRO's, Investigator sites, Centralised Labs and specialist Non Clinical Labs. In this role insights and… more
- University of Rochester (Rochester, NY)
- …with IRB regulations. Will be responsible for ensuring the comfort, privacy, and informed consent of human subjects during experimental procedures by explaining ... members on the details for the protocol, including inclusion and exclusion criteria, informed consent procedures, and study activities. 40% + Manages, collects,… more
- Rush University Medical Center (Chicago, IL)
- …research to identify applicable practice guidelines will be required. * Review patient informed consent forms to ensure that the document accurately informs ... terms in the coverage analysis with the protocol, the informed consent form template, the budget and...Certifications may include: Certified Professional Coder (CPC), Certified Coding Specialist (CCS) and Certified Medical Coder (CMC), and any… more
- The Mount Sinai Health System (Jamaica, NY)
- …to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients, recalling patients for further evaluation ... the general nature and level of work performed by physician assistants and senior physician assistants in the Emergency Department. This should not be construed as… more
- The Mount Sinai Health System (Elmhurst, NY)
- …pursuant to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patient, recalling patients for further evaluation ... -Job requires completion of NYS-approved program for training of physician or specialist assistants to acquire knowledge of anatomy, physiology and clinical patient… more
- Randstad US (Cambridge, MA)
- …protocol development (such as contribution to writing of protocol and/or amendments, informed consent , committees charters development and other study ancillary ... guidance of the CRD he/she collaborates with the Coding specialist , Biostatisticians, Data Managers, Global and Regional Study Managers,...have: + Minimum Ph.D. or Pharm D + Previous senior clinical experience + Minimum of 5 years of… more