Clinical Research Nurse Coordinator
Location: Portsmouth Virginia
Description: Clinical Research Management, Inc. is at present looking to employ Clinical Research Nurse Coordinator right now, this vacancy will be placed in Virginia. Further informations about this vacancy opportunity please give attention to these descriptions. ClinicalRM is seeking a Clinical Research Nurse Coordinator to work at NMCP in Portsmouth, VA.
RESPONSIBILITIES:
2. Assign appropriate patient randomization number per protocol design.
3. Ensure that the consent process has taken place effectively and all questions are answered satisfactorily and documented.
4. In collaboration with the Research Pharmacist, ensure that drugs are correctly dispensed as per protocol.
5. Maintain accurate documentation record of drugs received.
6. Provide education to patients on compliance, possible side effects, drug interactions and importance of contacting the coordinator.
7. Process and prepare specimens for lab analysis and shipping.
8. Observe universal precautions and Occupational Safety & Health Administration (OSHA) standards when processing or handling specimens.
9. Monitor laboratory results and consult with the PI for follow-up care.
10. Collect data in a timely and accurate manner and submi! t information to coordinating centers as required.
11. Report adverse events to governing agencies and sponsors as required by protocol and regulations.
12. Evaluate compliance of research subject and complete documentation of status and progress.
13. Conduct telephone, face-to-face interviews or mail information for follow-up visits.
14. Maintain detailed documentation of the research study including but not limited to individual patient files, databases as required by the protocol and the Investigator's File Binder/Regulatory Binder.
15. Prepare reports and other correspondence regarding the research protocol for the IRB, granting agencies, industry sponsors and other organizations as required by regulation and/or the protocol.
16. Interact on a regular basis with the PI regarding the conduct of the research study.
17. Attend conferences and other meetings as required by the protocol, the PI or sponsoring agen! cy.
18. Maintain a safe workplace ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations.
19. Perform light duties and other related duties as required and assigned.
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If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to Clinical Research Management, Inc..
If you interested on this vacancy just click on the Apply button, you will be redirected to the official website
This vacancy starts available on: Thu, 25 Apr 2013 11:45:05 GMT
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