- Gilead Sciences, Inc. (Foster City, CA)
- …limited to the following:** + Tracks and and update project specific information in clinical trial management system, databases, and/or other tools + Assist with ... filing and review of study documents in the eTMF + Collaborates with cross functional teams and CROs/vendors to complete various day to day activities as assigned - such as develop study plans and facilitate review of the study plans + Review of monitoring… more
- MetroHealth (Cleveland, OH)
- …in accordance with study protocols. These may include observational or interventional trials . Upholds the mission, vision, values, and customer service standards of ... human subject research. Administrative support experience in a medical or clinical research setting. Institutional Review Board (IRB) experience. Certified … more
- UNC Health Care (Chapel Hill, NC)
- …**Job Details** Legal Employer: STATE Entity: UNC Faculty Physicians Organization Unit: Clinical Trials Unit Passthrough Work Type: Full Time Standard Hours ... Per Week: 40.00 Salary Range: $23.01 - $33.07 per hour (Hiring Range) Pay offers are determined by experience and internal equity Work Assignment Type: Hybrid Work Schedule: Day Job Location of Job: US:NC:Chapel Hill Exempt From Overtime: Exempt: Yes This is a… more
- UNC Health Care (Chapel Hill, NC)
- …**Job Details** Legal Employer: STATE Entity: UNC Faculty Physicians Organization Unit: Clinical Trials Unit Passthrough Work Type: Full Time Standard Hours ... Per Week: 40.00 Salary Range: $26.59 - $38.23 per hour (Hiring Range) Pay offers are determined by experience and internal equity Work Assignment Type: Hybrid Work Schedule: Day Job Location of Job: US:NC:Chapel Hill Exempt From Overtime: Exempt: Yes This is a… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …+ Knowledge of the PeopleSoft Financial System preferred. PREFERRED QUALIFICATIONS: + Clinical trials experience preferred. NOTE: This role will be granted ... the opportunity to work from home regularly but must be able to commute to Emory University location as needed and at times, on short notice. Emory reserves the right to change this status with notice to employee. \#LI-VJ1 **Additional Details** Emory is an… more
- MetroHealth (Cleveland, OH)
- …is done in accordance with physician's orders, study protocols, good clinical practice standards as well as approved/recognized standards of nursing care/nursing ... variety of settings, such as inpatient, ambulatory, and the Clinical Research Unit (CRU). Notifies the IRB of adverse...licensure in the State of Ohio. One year of clinical experience as a staff nurse or 2 years… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research ... studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains ... study requirements. + Assists in the activities related to clinical research studies including but not limited to: answering...data through chart reviews. + Secures, delivers and ships clinical specimens as required by the protocol. + Prepares… more
- Queen's Health System (Honolulu, HI)
- RESPONSIBILITIES I. JOB SUMMARY/RESPONSIBILITIES: * Conducts clinical research studies under the immediate direction of assigned Principal Investigator. * Assists ... researchers, clinical and administrative personnel in performing a variety of duties on a research project. II. TYPICAL PHYSICAL DEMANDS: * Essential: standing,… more
- University of Pennsylvania (Philadelphia, PA)
- …the accuracy of all study documentation. The coordinator will oversee 2 or more clinical trial ensuring that the integrity of the protocol is maintained, all ... CRC B is expected to manage 5 or more clinical trials . The CRC B will be...study documentation. The coordinator will oversee 2 or more clinical trial ensuring that the integrity of… more