- Antech Diagnostics (Lake Success, NY)
- …relevant job-related skills, experience, education, training and budget.** **Job Purpose/Overview:** The Clinical Studies Coordinator is an experienced ... along with external collaborations and internal sample acquisition. The Clinical Research Associate and Coordinator with be... with be responsible for working closely with the Clinical Studies Director on the Medical Affairs… more
- MD Anderson Cancer Center (Houston, TX)
- The primary purpose of the Clinical Studies Coordinator is to provide clinical study related coordination including but not limited to data management, ... regulatory offices, and patients to maintain and ensure the smooth operation of clinical studies within a Phase I study or single patient IND (SPIND). **JOB… more
- MD Anderson Cancer Center (Houston, TX)
- The Coordinator , Clinical Studies - Regulatory ensures regulatory compliance for the Department of Genitourinary Medical Oncology clinical trials, ... information and develops and/or designates educational presentations for the monthly Clinical Research Group (CRG) meetings and Data Coordinator /Research Nurse… more
- MD Anderson Cancer Center (Houston, TX)
- …cancer centers designated by the National Cancer Institute. The primary purpose of the Coordinator , Clinical Studies is to provide clinical evaluation, ... presented at weekly training meetings. **2. Coordination of regulatory correspondence on clinical research studies .** . Communicate verbally and in writing, as… more
- MD Anderson Cancer Center (Houston, TX)
- …trainees, professionals, employees and the public. The primary purpose of the Senior Coordinator , Clinical Studies position is to collaborate with the ... research. Under the guidance of the Research Nurse Supervisor, the Senior Coordinator , Clinical Studies will also assist with the supervision of data… more
- MD Anderson Cancer Center (Houston, TX)
- …Activities Participate in protocol-specific clinical tasks as needed. Guide the clinical studies coordinator on research-related processes for patients ... field. Three years of Supervisory/management experience is preferred. **Preferred Experience:** Sr. Clinical Studies Coordinator experience at MD Anderson.… more
- University of Pennsylvania (Philadelphia, PA)
- …recruitment and enrollment, study visits and regulatory compliance in one or more studies . Clinical Research Coordinator work includes study design, protocol ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator - A/B (Department of Translational Medicine and Human… more
- University of Pennsylvania (Philadelphia, PA)
- …observational and retrospective studies , and include single-site and multi-site studies . Clinical Research Coordinator A: Coordinate Phase 0-III ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Department of Pathology and Laboratory Medicine)… more
- Mount Sinai Health System (New York, NY)
- …supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, ... involving genetic tests. 7. Independently obtains informed consent for other clinical studies . 8. Mentors Clinical Research Coordinators in training. 9.… more
- University of Colorado (Aurora, CO)
- … studies are in stock and in working order + Act as a Primary Clinical Research Coordinator on multiple studies + Independently master study materials, ... ** Clinical Research Coordinator (Open Rank: Entry...studies to ensure compliance with study protocols, department, hospital/ clinical standard operating procedures, and other regulatory guidelines +… more