- SUNY Upstate Medical University (Syracuse, NY)
- …Review Board and regulatory agencies. Enroll, register and screen patients for clinical research trials; collect and submit clinical trial patient data. ... proper collection and shipment of lab samples; billing support; maintenance of clinical research study supplies and drug accountability. Minimum Qualifications:… 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...research setting. * Experience to demonstrate knowledge of research regulatory processes (human subject protection, biological… more
- SUNY Upstate Medical University (Syracuse, NY)
- …of education and experience. SoCRA certified or ACRP certified Experience with clinical research protocols, knowledge of medical terminology, computer skills, ... Job Summary: Position is Project Manager for a large multi-site clinical trial. Train and oversee CRA's on the project. Clinical Site is also Coordination Center… more
- BeOne Medicines (Emeryville, CA)
- …site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ... ICH-GCP guidelines, local regulations, and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study… more
- ICON Clinical Research (TX)
- As a CRA you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be ... Act as the primary contact and facilitate efficient communications between the clinical trial team and the sites + Perform remote and on-site… more
- AbbVie (Montgomery, AL)
- …Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research . Stay abreast of new and/or evolving local regulations, ... that could affect timelines and develop alternative solutions. + Ensure clinical trial management systems containing all site-specific information are maintained and… more
- SUNY Upstate Medical University (Syracuse, NY)
- …and experience. Preferred Qualifications: Two years of experience in a cardiology clinical research . Work Days: M-F Daytime Hours Message to Applicants: ... primary function of this position is to assist the investigators in their research studies within the Cardiology Division of the Department of Medicine. This… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: This role will act as the project manager for a large multi-site clinical trial where the clinical site is also the coordination center for the ... clinical trial. Duties include but are not limited to:...deviation reporting and management, communication and periodic reporting to regulatory agencies and financial sponsors, secure and track all… more
- Johns Hopkins University (Baltimore, MD)
- …supervises, and evaluates the employees working in the OCT including but not limited to Clinical Research Regulatory Specialists, Clinical Research ... methods used to regulate the efficiency and conduct of clinical research activities, including regulatory ,... research teams. + Provides metrics to Senior Associate Dean for Clinical Trials, the Vice… more
- Rush University Medical Center (Chicago, IL)
- …**Certifications:** * Certified Clinical Research Professionals (CCRP), * Certified Clinical Research Associate (CCRA), * Certified Clinical ... or training. **Preferred Job Qualifications:** **Experience:** * 2-5 years' experience in clinical research conduct, regulatory management, or research… more
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