- Penn State Health (Hershey, PA)
- …The research nurse may evaluate and analyze clinical data. The Research RN will monitor study activities to ensure compliance with protocols and will ... Research RN will plan, direct, or coordinate clinical research projects. The Research ...all relevant local, federal and state regulatory and institutional policies. **MINIMUM QUALIFICATION(S):** + Bachelor's degree… more
- Touro University (Hawthorne, NY)
- … team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research . + Monitor study patients for adverse events in collaboration ... pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment,...to ensure protocol compliance in conjunction with the PI, clinical team and clinical research … more
- Actalent (Detroit, MI)
- …patients, and regulatory personnel to ensure the successful execution of clinical research studies. Key Responsibilities + Coordinate and manage oncology ... Oncology Clinical Research Coordinator Job Description The... regulatory agencies. + Ensure compliance with all regulatory requirements and Good Clinical Practice (GCP)… more
- St. Luke's Health System (Boise, ID)
- …2 years' experience **Preferred Qualifications:** + Strong background in oncology or clinical research + Working knowledge of medical and scientific terminology ... data submission via the appropriate mechanism. + Assists in recruiting patients for clinical trials. + Conducts research activities per protocol. + Documents … more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Interacts with investigators and their staff to facilitate and monitor the conduct of multidepartment clinical studies.… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B (Department of Endocrinology,Diabetes and Metabolism) Job ... Profile Title Clinical Research Coordinator B Job Description Summary...solutions. Implement approved changes to procedures as needed and monitor results. Responsible for study recruitment and coordination/ conduction… more
- St. Luke's Health System (Boise, ID)
- …data submission via the appropriate mechanism. + Assists in recruiting patients for clinical trials. + Conducts research activities per protocol. + Documents ... to physicians, investigators and other staff members for questions regarding the research process. + Collaborates with investigator and regulatory staff… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The primary function of this position is to serve as the Clinical Research Coordinator for multiple projects within the institution, under the ... Qualifications: Office Experience including computer experience- Excel, Word and some Power Point Clinical Research Experience with the ability to work on their… more
- Northwell Health (Manhasset, NY)
- …ships specimens according to protocol and training requirements. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, ... and supply companies, as needed. + Adheres to good clinical practice, and complies with regulatory and...experience. + 1-3 years of relevant experience, required. + Clinical trials experience, preferred. + Scientific research … more
- BeOne Medicines (San Mateo, CA)
- **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... 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