- MD Anderson Cancer Center (Houston, TX)
- The primary purpose of the Manager , Clinical Protocol Administration position is to lead and collaborate with the research team and Principal ... and evaluation process of the Data Team. Coordinates schedules, training and protocol assignments for Data Team beginning at clinical concept presentation.… more
- General Dynamics Information Technology (Lackland AFB, TX)
- …Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a Senior Clinical Research Administration Manager to support research within the ... Degree with 5+ years of experience in medical research, human subjects research protocol administration OR Master's in a scientific field can substitute for… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Cerebrovascular Division Manager , Clinical Administration within the Comprehensive Stoke Center assesses and institutes optimal patient ... + Leads and directs Division interdepartmental Comprehensive Stroke Center operations. **_OR Clinical Manager - OR neurovascular tech team:_** + Directs daily… more
- Mount Sinai Health System (New York, NY)
- **Job Description** We are seeking a Clinical Program Manager (CPM) to join a team of investigators and advanced practitioners who are dedicated to delivering ... the protocol is conducted in a high-quality manner and clinical research documentation is inspection ready. + Responsible for coordinating study enrollment,… more
- Mount Sinai Health System (New York, NY)
- …in the administration and plan of the research program. The Clinical Program Manager will report into Associate Director. **Qualifications** Education: + ... **Job Description** The Clinical Program Manager provides clinical...Works with Clinical Research Coordinators and other clinical staff to ensure protocol compliance, accurate… more
- Vanderbilt University Medical Center (Nashville, TN)
- …programs in patient care, education, and research. **Organization:** VICTR **Job Summary:** Clinical Trials Manager - VICTR - Vanderbilt Coordinating Center ... (VCC) JOB SUMMARY In your pivotal role as a Clinical Trials Manager , you will be supporting...Clinical Trial by reviewing Serious Adverse Event reports, Protocol Deviations, and other unanticipated events that occur at… 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
- Harvard University (Cambridge, MA)
- …related discipline. + Three or more years of related experience which must include clinical research administration or clinical research, or a combination of ... Skills: + Experience working with Institutional Review Boards for human clinical studies including protocol generation, continuing review, enrollment tracking,… 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
- 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
- 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
- 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
- Veterans Affairs, Veterans Health Administration (Charleston, SC)
- …Description Title/PD#: Health System Specialist - Research Committee Manager /PD99586S Physical Requirements: Primarily sedentary, some slight physical effort ... may be required. Major Duties: Serves as the Program Manager and Specialist for multiple regulatory committees as expert in activities related to animal, basic… more
- University of Florida (Gainesville, FL)
- …Grant or Research Administration , Nursing, Health Care Administration /Support Department: 29040100 - MD-ANESTHESIOLOGY-GENERAL Classification Title: Clinical ... and comprehend the protocol and collaborate with the PI and research manager to prepare IRB and any other regulatory submission documents. * Prepare other study… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …RESPONSIBILITIES: + This is a central job, reporting to the Office for Clinical Research (OCR). + Responsible for the Prospective Reimbursement Analysis (PRA) for ... 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
- 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
- University of Washington (Seattle, WA)
- …**The Division of General Internal Medicine has an outstanding opportunity for a Clinical Research Program Manager to join their team.** The University of ... of Medicine - Tsui Research Program, has an outstanding opportunity for a Clinical Research Program Manager . This individual will be responsible for the… more
- University of Florida (Lake County, FL)
- …categorized budget and justification. Regulatory and IRB + Reviews and comprehends the protocol . + Collaborates with the PIand research manager (s)to prepare IRB ... protocol management. Reporting + Assists Principal Investigator andresearch manager (s)with scientific and compliance reporting requirements in accordance with… more
- University of Miami (Miami, FL)
- …and service while ensuring population-specific patient care and compliance with the research protocol in an ambulatory setting. The Clinical Trials Nurse, Level ... and documents adverse events and concomitant medications. Works closely with the protocol University Clinical Research Staff to ensure Serious Adverse Events… more