| Research Nurse Coordinator -- Shrewsbury, MA |
Author: Jon Merz
Date: 05-09-11 21:03
20102-Research Nurse Coordinator
GENERAL SUMMARY OF POSITION:
Under the direction of the Principal Investigator or designee the Research Nurse Coordinator I is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs devices or research inventions. The Research Nurse Coordinator I is a primary resource for study protocol conduct acting as a liaison between the Principal Investigator institutional review board (IRB) and sponsor to ensure good clinical practice standards (GCP) throughout the life cycle of the study.
Additional Information:
Clinical research experience preferred
RN required, NP or PA welcome
Potential to full time in the future
MAJOR RESPONSIBILITIES:
* Assist the Principal Investigator in feasibility and budget assessments for research studies
* Organize and maintain appropriate regulatory documents in accordance with sponsor and institutional standards throughout the life of the study
* Screen patients according to study criteria randomize enroll and consent in accordance with GCP standards
* Schedule perform and/or coordinate all study procedures according to protocol requirements and sponsor conventions
* Identify adverse events according to study standards; triage report and document with the Principal Investigator according to IRB and sponsor requirements
* In collaboration with the investigational pharmacy ensure proper adherence to randomization schema study drug dosing and administration per protocol
* Perform nursing assessments of study participants according to protocol and consult with clinician or Principal Investigator as necessary
* Document and record in writing or electronically all study events and protocol related procedures
* Review and abstract medical record information in a consistent manner in accordance with study protocol institutional and HIPAA requirements
* Maintain patient/subject confidentiality and strictly adhere to all federal state and institutional standards for GCP
* Maintain business confidentiality as it relates to sponsor protocol and related regulatory documents
* Attend meetings conferences and seminars as required
* Adhere to all institutional health safety and infections control regulations and requirements
* Adhere to the policies and procedures of any clinical site where study is being performed
* Perform additional duties as trained and required by study protocols
* Perform other duties as required.
MINIMUM QUALIFICATIONS:
* RN with current registration to practice nursing in Massachusetts
* 3 years of relevant nursing experience
* Phlebotomy and EKG skills preferred
* Demonstrated Microsoft office skills
* Strong oral and written communication skills attention to detail is essential
* Ability to work in a team environment to facilitate the integrity of the study and its timely completion
* Ability to travel to off-site locations
To apply: Visit our website at www.umassmed.edu, click on Human Resources, Job Opportunities, Search for Req # 20102
As an equal opportunity and affirmative action employer, UMMS recognizes the power of a diverse community and encourages applications from individuals with varied experiences, perspectives and backgrounds.
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Author |
Date |
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Research Nurse Coordinator -- Shrewsbury, MA |
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Jon Merz |
05-09-11 21:03 |
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