- Stanford University (Stanford, CA)
- …staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies . + Develop and manage ... and maintain follow-up for children and adults in Pediatric CCT studies . We are seeking candidates with excellent communication, organization, prioritization,… more
- Beth Israel Lahey Health (Burlington, MA)
- …the study team: + Implements, conducts and coordinates assigned research studies by reviewing all pertinent study documents and assessing departmental and ... Under general supervision and direction provides direct care to research study participants and makes necessary nursing judgments. Performs diverse administrative… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …of plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies . Ensure consistency ... timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard… more
- Abbott (Alameda, CA)
- …is onsite in our Alameda, CA location. **What you'll work on** + Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of ... clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations,… more
- University of Pennsylvania (Philadelphia, PA)
- …preparing trials for audits and inspections. The CRC will participate in study team meetings and ongoing protocol training/compliance meetings and will be expected ... the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing...of the federal regulations for the conduct of clinical studies and human subject protection. + Act in lead… more
- Stanford University (Stanford, CA)
- …set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. He/she will ... Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local,… more
- University of Pennsylvania (Philadelphia, PA)
- …Clinical Research Coordinator to organize, coordinate and implement complex cancer studies involving a wide variety of investigational products and various sponsors. ... the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol… more
- University of Rochester (Rochester, NY)
- …to research studies and designs. + Implements and monitors resulting study changes. Other duties as assigned. **MINIMUM EDUCATION & EXPERIENCE** + Bachelor's ... subject research activities, which may include multiple site human subject studies . May provide training on federal, state, sponsor and/or institutional regulations,… more
- University of Pennsylvania (Philadelphia, PA)
- …and (2) meet required obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report directly to the ... (but are not limited to): + Plan, organize, and contribute to study -related meetings, including but not limited to Investigator Meetings, Site Initiation Visits,… more
- Vitalief (Newark, NJ)
- …research center in Newark, NJ, managing high-priority interventional oncology clinical studies across multiple disease groups. WHY VITALIEF? + Contribute to ... with experience). RESPONSIBILITIES: + Under the direction of the Clinical Research Study Site Leader, support the planning, implementation, and execution of multiple… more