- MD Anderson Cancer Center (Houston, TX)
- …and TMC regulatory area to be aware of upcoming protocols. . Participate in protocol -specific clinical tasks as needed. . Oversee activities of HAL clinical ... professionals, employees and the public. **JOB SPECIFIC COMPETENCIES** **1.** ** Administration and Management** **50%** . Provides administrative management of the… more
- University of Southern California (Los Angeles, CA)
- …/Off Study of patients. 9. Assists in training of other Coordinators. B. Protocol Administration 1. Determines patient eligibility a. Schedules necessary tests. ... experienced Registered Nurse and has a strong interest in clinical research. The role of the protocol ...for reporting to the IRB and promptly notifies Data Manager of occurrence of SAE. 5. Interacts with the… more
- University of Pennsylvania (Philadelphia, PA)
- …Job Title Clinical Research Coordinator A/B (Department of Surgery Research Administration ) Job Profile Title Clinical Research Coordinator A Job Description ... Summary The CRC A will assist in the management of multiple clinical trials and responsibilities in specific research area. Coordinate the screening of patients,… more
- University of Colorado (Aurora, CO)
- Clinical Science Program Manager - 33067 University Staff **Description** **University of Colorado Anschutz Medical Campus** **School of Medicine | Department of ... Medicine** **Job Title:** ** Clinical Science Program Manager ** **Position: #00821011 -...coordination and regulatory processes, procedures as defined in study protocol and in compliance with regulating bodies, including but… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (Surgery Research Administration ) Job Profile Title ... Description Summary This position will assist in the management of multiple clinical trials and responsibilities in specific research area. Coordinate the screening… more
- Veterans Affairs, Veterans Health Administration (St. Cloud, MN)
- …professional mental health counselor (LPMHC) assigned to the Mental Health Integrated Clinical Community (MH ICC) spending a portion of time providing various ... i. The incumbent will provide a full range of clinical services which includes case work, individual, family and...assignments, as deemed necessary by the MH Special Programs Manager . n. The incumbent will maintain data and statistical… more
- Veterans Affairs, Veterans Health Administration (Iron Mountain, MI)
- Summary He/she serves as a leader in the Clinical Video Teleconferencing (CVT) Program and oversees the performance of staff at the parent facility and its ... the care coordinator, monitoring weekly appointments and staffing, LPN alerts Nurse Manager (or designee) when conflicts arise. The LPN successfully and consistently… more
- Johns Hopkins University (Baltimore, MD)
- The Department of Neurology is seeking a ** Clinical Trials Project Manager ** (CTPM) to join the research team in the division of Neuroimmunology. The Manager ... processes to increase referrals and increase accruals to multiple clinical trials + Track each protocol through...+ Function as a liaison with the IRB and Clinical Research Office and other research administration … more
- Albany Medical Center (Albany, NY)
- …DUTIES AND RESPONSIBILITIES - and as supervised under PI / Research Manager /RN oversight where appropriate: Complete and submit protocol specific research ... soundness and logistical capabilities as appropriate Knowledgeable on each protocol 's specific inclusion, exclusion, therapy, clinical monitoring oversight,… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Manager (CRM) is responsible for the day to day oversight and management of Clinical Trials Office clinical ... activity to ensure compliance with Standard Operating Procedures and Good Clinical Practices. **JOB DUTIES AND RESPONSIBILITIES:** **Oversight of assigned study… more
- Johns Hopkins University (Baltimore, MD)
- …experience in clinical research and regulatory affairs. + Experience in protocol and informed consent writing, data analysis, grant writing, and /or manuscript ... financial management of clinical trials preferred. Classified Title: Clinical Research Program Manager Role/Level/Range: ACRP/04/MD Starting Salary Range:… more
- Rush University Medical Center (Chicago, IL)
- …while ensuring the protocol is conducted in a high-quality manner. Educates clinical staff and physicians regarding study. Updates clinical staff on study ... while ensuring the protocol is conducted in a high-quality manner. Educates clinical staff and physicians regarding study. Updates clinical staff on study… more
- Actalent (Washington, DC)
- …and compliance. + Ensures, reviews, and quality controls against associated project protocol , NIAID requirements, CRF standards templates, Good Clinical Data ... of 5 years of supervisory and operational management experience required. + Certified Clinical Data Manager (CDM) certification preferred. + Expert in multi-site… more
- Actalent (Bethesda, MD)
- …and compliance. Ensures, reviews, and quality controls against associated project protocol , NIAID requirements, CRF standards templates, Good Clinical Data ... of 5 years of supervisory and operational management experience required. Certified Clinical Data Manager (CDM) certification preferred. Expert in multi-site … more
- Children's Hospital Boston (Boston, MA)
- 74507BRJob Posting Title: Clinical Research Manager IDepartment:Medicine-Hematology/OncologyAutoReqId:74507BRStatus:Full-TimeStandard Hours per Week:40 Job ... the Dana-Farber/Boston Children's Cancer and Blood Disorders Center is seeking a clinical research manager . Ground-breaking research within the group focuses on… more
- Northwell Health (Glen Oaks, NY)
- **Req Number** 108864 Job Description Provides management of research administration at a clinical site(s) including monitoring the quality and accuracy of ... for clinical research sites for questions related to the protocol conduct protocol , regulatory document completion, study supplies, client scheduling,… more
- University of Pennsylvania (Philadelphia, PA)
- … trial meets expectations and that they are conducted in accordance with the specific clinical protocol as approved by the Sponsor, study team and in accordance ... and resources, and much more. Posted Job Title Project Manager A/B (Penn Infectious Diseases Clinical Research...performance management, and development of key study documents including protocol , consent, and CRFs. The Project Manager … more
- University of Florida (Lake County, FL)
- …and comprehends the protocol . + Collaborates with the PI and research manager (s) to prepare IRB and any other regulatory submission documents as required by the ... Clinical Research Coordinator III Apply now (https://secure.dc4.pageuppeople.com/apply/674/gateway/default.aspx?c=apply&lJobID=519679&lJobSourceTypeID=796&sLanguage=en-us) Job… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …health-related or business administration program required and seven (7) years of clinical research experience, with at least four (4) years of Clinical ... DESCRIPTION: + Responsible for directing and managing large and highly complex clinical research groups. + With support from operational leadership, assesses team… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …DESCRIPTION: + This is a central job, reporting to the Office for Clinical Research (OCR). Responsible for the Prospective Reimbursement Analysis (PRA) for all ... complex study protocols, Informed Consent Documents (ICD), draft sponsor Clinical Trial Agreements (CTA), and budgets to identify all...(IND). + Verifies the IND status in the study protocol , eIRB, or FDA study documentation. + Evaluates Category… more