• New London
• US$65000 - US$75000 per year
• Posted 1 day ago

Position Overview: In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and monitor patient status and safety; collect and organize research data; schedule and conduct study-specific training and site in-services to study related s...

• Overland Park
• US$40000.00 - US$55000.00 per year
• Posted 3 days ago

Summary Of Responsibilities: We are seeking a dedicated and detail-oriented Clinical Research Assistant to support our research team in a dynamic clinical setting. This role involves working directly with patients, assisting research staff with clinical trial activities, and ensuring adherence to...

• Aurora
• US$60000 - US$75000 per year
• Posted 3 days ago

Overview Responsibilities Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol. Coordinates patient care in compliance with protocol requirements. May disburse inves...

• Edgewood
• US$25.00 - US$40.00 per hour
• Posted 10 days ago

Responsibilities/ Job Duties: Clinical Research Nurse (CRN) Responsibilities, as delegated by the Principal Investigator (if required): a) Standard Clinical Research Coordinator tasks b) Phlebotomy (peripheral veins only) c) Non-invasive sample collection (mouth swab, urine, sputum, etc.) d) Perf...

• Syracuse
• US$45 - US$60 per hour
• Posted 14 days ago

We are looking for reliable and hard working RNs to join the Upstate Specialty Services at Harrison Center for multiple RN opportunities in Syracuse, NY. If you are interested in learning more, APPLY NOW! Location: Address: 550 Harrison St, Syracuse, NY 13202 (Upstate Specialty Services at Harris...

• West Bend
• US$80000.00 - US$90000 per year
• Posted 16 days ago

Overview: This position involves overseeing daily operations on the clinical study floor during shifts, ensuring all clinical trials run smoothly and patients are cared for in a calm, professional environment. You'll work with a supportive team and gain valuable experience in clinical research wh...

• Sacramento
• US$31 - US$43 per hour
• Posted 18 days ago

Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with FDA, GCP, and ICH Guidelines. Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. I...

• Firestone
• US$60000.00 - US$90000 per year
• Posted about 1 month ago

Overview Responsibilities Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol. Coordinates patient care in compliance with protocol requirements. May disburse inves...

• Federal Heights
• US$95000.00 - US$110000 per year
• Posted about 1 month ago

Responsibilities Oversees the research and clinical operations for all nursing clinical support activities Establishes and maintains all nursing personnel files. Ensures all licensing and certification criteria are met. Assists with the review and revision of clinical policies and procedures. Ens...

• Denver
• US$55 - US$70 per hour
• Posted about 1 month ago

*Must have both hospitalist & Oncology experience* - Assesses, plans, implements, and evaluates care for patients- patients will primarily be those involved in ongoing oncology research trials - Initiates and documents appropriate interventions; evaluates and records patient/family response and p...

• New Britain
• US$55000.00 - US$75000.00 per year
• Posted about 1 month ago

JOB SUMMARY A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, rep...