- George Washington University (Washington, DC)
- … Trials Management System (CTMS). Acts as a communication liaison between GW OCR, clinical study staff, and internal and external customers during the ... for all industry supported clinical trials and clinical research. Dedicated Research Program Manager of...across Phases II-IV and ICH GCP Good understanding of clinical research trial protocols, associated study specifications,… more
- George Washington University (Washington, DC)
- I. JOB OVERVIEW Job Description Summary: The Program Manager is primarily responsible for administering and managing international programs for students and faculty ... of SMHS, including international clinical and research electives for students and residents, scholarships,...Master's degree or higher in a relevant area of study . Degree must be conferred by the start date… more
- Stanford University (Stanford, CA)
- Network Clinical Research Manager ( Hybrid ), Cancer Center South and East Bay **School of Medicine, Stanford, California, United States** Research Post Date 2 ... Clinical Research Manager - Cancer Center South and East Bay ( Hybrid Work Arrangement)** The Stanford Cancer Institute's Clinical Trials Office (SCI-CTO)… more
- Stryker (Mahwah, NJ)
- …precision. **What you will do** As the ** Clinical Study Manager (CSM),** you will manage ongoing Investigator-Initiated Studies and/or Stryker Initiated ... Study Manager ** to support Joint Replacement Clinical Trials. This role will be based ** hybrid...research strategy. + Develop and maintain overall dashboard of clinical and non- clinical studies , including… more
- Stryker (Cary, IL)
- …patients annually. More information is available at www.stryker.com We are currently seeking a ** Clinical Study Manager ** , to join our **Medical** Division. ... regulations and expectations. **What you will do** As a ** Clinical Study Manager ** , you... clinical regulatory documentation preparation and submissions for clinical studies (eg, IDE submissions, IRB/EC submissions).… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …Manager will:** + Lead all aspects of the planning and execution of IVD clinical studies , including study timeline development, to ensure that results are ... study registration updates (ct.gov or global registrations for clinical studies conducted outside of the United...Three (3) or more years of experience handling IVD clinical research studies from study … more
- UCLA Health (Los Angeles, CA)
- … Clinical Data Manager will be responsible for data management of clinical research studies . You will collect and transcribe research patient data and ... - $52.53Qualifications Required: * Bachelor's degree or 1-3 years of previous study coordination or clinical research coordination experience * Strong verbal… more
- ConvaTec (Lexington, MA)
- …regulations. **Key responsibilities and authority:** + Proactively manage assigned clinical studies . + Support clinical study delivery across Clinical ... Join us on our journey to #ForeverCaring as a Clinical Study Management Specialist, and you'll do...Role:** Provide operational expertise to ensure effective delivery of clinical studies across Convatec's Business Units. Reporting… more
- Taiho Oncology (Princeton, NJ)
- …+ Coordinates cross functional study team meetings and supports study manager with meeting minutes for assigned studies . + Updates internal study ... it most. This is an exciting opportunity to support clinical studies and experience multiple facets of...site-related documentation, and inspection readiness. + Collaborates closely with study manager to align expectations and … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …for this role. The position can be based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports the Clinical ... sites may be required to assist with monitoring clinical studies . **A typical day as CSAM...like:** + Lead/oversee the planning and management of a clinical study in an assigned region(s) in… more
- International Rescue Committee (New York, NY)
- Requisition ID: req45075 Job Title: Clinical Program Manager , Home Study and Post-Release Services Sector: Social Work Employment Category: Fixed Term ... 82,000.00 Annually Location: New York, NY HQ USA Work Arrangement: Hybrid Job Description SCOPE OF WORK: The IRC's Home... Job Description SCOPE OF WORK: The IRC's Home Study and Post-Release Services (HSPRS) for unaccompanied children in… more
- MD Anderson Cancer Center (Houston, TX)
- …. Under supervision of the protocol primary investigator (PI), the research nurse manager and/or clinical studies supervisor, assumes responsibility for the ... **JOB SPECIFIC COMPETENCIES** **Coordination of Study initiation and Operations of Clinical ...participating institutions and coordinates all data pertaining to such studies . . Sets up monitoring visits - Schedules the… more
- MD Anderson Cancer Center (Houston, TX)
- **Summary** The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol ... Excel, and others as designated. . Consults with PI and the Research Nurse Manager regarding ongoing study assignments. Collaborates with other members of the… more
- MD Anderson Cancer Center (Houston, TX)
- The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, ... Excel, and others as designated . Consults with PI and the Research Nurse Manager regarding ongoing study assignments. Collaborates with other members of the… more
- MD Anderson Cancer Center (Houston, TX)
- The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, ... Excel, and others as designated. * Consults with PI and the Research Nurse Manager regarding ongoing study assignments. Collaborates with other members of the… more
- MD Anderson Cancer Center (Houston, TX)
- …protocol specific duties under direct supervision of protocol PI, research nurses manager /supervisor. *Obtains consent for research studies *Assist in screening ... professionals, employees and the public. **JOB SPECIFIC COMPETENCIES** **Coordination clinical and translational research protocols** *Develops and maintains a… more
- MD Anderson Cancer Center (Houston, TX)
- The primary purpose of the Clinical Studies Coordinator is to provide all study related coordination for a position supporting Melanoma Medical Oncology and ... research nurses, and data managers to document patient care. * Coordinates with clinical research technicians and lab manager regarding scheduling of cell… more
- Merck (North Wales, PA)
- …operational responsibilities for a single study or across multiple studies (eg, operational deliverables, clinical & ancillary supplies planning/tracking, ... with team members. + May interact with internal and external stakeholders (eg, study team, vendors, committees) in support of clinical trial objectives. … more
- MD Anderson Cancer Center (Houston, TX)
- Coordinator, Clinical Studies MISSION STATEMENT The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, ... assignments as needed/requested. EDUCATION Ensures the conduct of assigned studies is in accordance with Good Clinical ...protocol related data and provide protocol guidance to the Clinical Study and Research Data Coordinators. SAMPLE… more
- University of Pennsylvania (Philadelphia, PA)
- …under general supervision. Assist CTT program manager with initiating study procedures for new industry-sponsored and investigator-initiated clinical trials. ... website (https://coronavirus.upenn.edu/) for the latest information. Posted Job Title Clinical Research Coordinator B/C ( Hybrid Eligible)(Abramson Cancer Center)… more
