- Beth Israel Lahey Health (Boston, MA)
- …Liaises with the IRB as needed; handles IRB inquiries regarding coordination between the informed consent form and the agreement. + Provides prompt and regular ... of the Associate Director of the Clinical Trials Office (CTO), the Senior Contracting Specialist works with investigators, clinical trial coordinators and… more
- Texas Tech University (Lubbock, TX)
- …monitoring visits of human research protocols, review protocol regulatory documents, informed consent process and data collection. Conduct independent ... **37333BR** **Extended Job Title:** Senior Research Compliance Specialist **Position Description:** Performs specialized compliance activities related to… more
- Kestra Medical Technologies, Inc (Kirkland, WA)
- …results + Prepare clinical study documentation such as the protocols, case report forms, informed consent form, and training materials + Oversee all aspects of ... clinical data management including electronic data capture (EDC) system and data entry + Establish and manage working relationships with contract research organizations (CRO), clinical site investigators and research staff + Work collaboratively with… more
- University of Colorado (Aurora, CO)
- …performed + Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for ... of subject to participate in clinical trial + Perform informed consent process or ensures that the...CU Department of Dermatology's Clinical Research Unit seeks a senior study specialist (Clinical Research Specialist… 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
- Weill Cornell Medical College (New York, NY)
- …and guidelines and internal SOPs. + Assists with eligibility assessment and informed consent process, as appropriate. Performs central subject registration for ... Title: Clinical Research Specialist -CCTO Location: Upper East Side Org Unit: GU...exposure to a team research environment at all levels ( senior investigators, nurses, research coordinators, lab technicians). **Knowledge, Skills… 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
- State of Minnesota (St. Paul, MN)
- …General Merchandise Buyer/Copy Center Manager** **Job Class: Central Services Administrative Specialist , Senior ** **Agency: Minnesota State** + **Who May Apply** ... to buy. + Ability to create relationships to make informed buying decisions that represents the campus community. +...to conform to Minnesota State's vehicle use criteria and consent to a Motor Vehicle Records check. AN EQUAL… more
- ConvaTec (Lexington, MA)
- …study documentation including Clinical Investigation Plan (CIP), Investigator Brochure (IB), Informed Consent Form (ICF) and Clinical Study Report (CSR). ... Join us on our journey to #ForeverCaring as a Clinical Study Management Specialist , and you'll do the same. **About the Role:** Provide operational expertise to… more
- University of Rochester (Rochester, NY)
- …staff on details of study activities, including inclusion and exclusion criteria, informed consent procedures, process for source documentation and case report ... PURPOSE: We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our...to develop robust study protocols and clear and accessible consent forms that prioritize inclusivity and comprehension for older… 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
- 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
- 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